DMD Rabbit Polyclonal Antibody

DMD Rabbit Polyclonal Antibody

To Order Contact Us Below:

    Mouse Dystrophin (DMD) ELISA Kit
    RDR-DMD-Mu-48Tests 48 Tests
    EUR 640.8

    Mouse Dystrophin (DMD) ELISA Kit
    RDR-DMD-Mu-96Tests 96 Tests
    EUR 890.4

    DMD Polyclonal Antibody
    ES9017-100ul 100ul
    EUR 334.8
    Description: A Rabbit Polyclonal antibody against DMD from Human/Mouse/Rat. This antibody is tested and validated for IHC

    DMD Polyclonal Antibody
    ES9017-50ul 50ul
    EUR 248.4
    Description: A Rabbit Polyclonal antibody against DMD from Human/Mouse/Rat. This antibody is tested and validated for IHC

    DMD Polyclonal Antibody
    ABP58391-003ml 0.03ml
    EUR 189.6
    Description: A polyclonal antibody for detection of DMD from Human, Mouse, Rat. This DMD antibody is for IHC-P. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human DMD protein

    DMD Polyclonal Antibody
    ABP58391-01ml 0.1ml
    EUR 346.8
    Description: A polyclonal antibody for detection of DMD from Human, Mouse, Rat. This DMD antibody is for IHC-P. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human DMD protein

    DMD Polyclonal Antibody
    ABP58391-02ml 0.2ml
    EUR 496.8
    Description: A polyclonal antibody for detection of DMD from Human, Mouse, Rat. This DMD antibody is for IHC-P. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human DMD protein

    DMD Rabbit pAb
    A1411-100ul 100 ul
    EUR 369.6

    DMD Rabbit pAb
    A1411-200ul 200 ul
    EUR 550.8

    DMD Rabbit pAb
    A1411-20ul 20 ul
    EUR 219.6

    DMD Rabbit pAb
    A1411-50ul 50 ul
    EUR 267.6

    Polyclonal DMD / Dystrophin Antibody
    APR11762G 0.05mg
    EUR 580.8
    Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human DMD / Dystrophin . This antibody is tested and proven to work in the following applications:

    Rabbit DMD ELISA Kit
    ERTD0036 96Tests
    EUR 625.2

    DMD Antibody
    1-CSB-PA503789
    • EUR 380.40
    • EUR 292.80
    • 100ul
    • 50ul
    Description: A polyclonal antibody against DMD. Recognizes DMD from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:1000-1:2000, IHC:1:25-1:100

    DMD Antibody
    1-CSB-PA006963GA01HU
    • EUR 716.40
    • EUR 399.60
    • 150ul
    • 50ul
    Description: A polyclonal antibody against DMD. Recognizes DMD from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB

    DMD Antibody
    1-CSB-PA006963LA01HU
    • EUR 380.40
    • EUR 402.00
    • 100ug
    • 50ug
    Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC; Recommended dilution: IHC:1:200-1:500

    DMD antibody
    70R-16862 50 ul
    EUR 522
    Description: Rabbit polyclonal DMD antibody

    DMD Antibody
    36428-100ul 100ul
    EUR 302.4

    Dystrophin (DMD) Polyclonal Antibody (Human)
    4-PAB503Hu01
    • EUR 286.80
    • EUR 2869.20
    • EUR 717.60
    • EUR 358.80
    • EUR 253.20
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD)

    Dystrophin (DMD) Polyclonal Antibody (Mouse)
    4-PAB503Mu01
    • EUR 291.60
    • EUR 2948.40
    • EUR 735.60
    • EUR 366.00
    • EUR 254.40
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD)

    Rabbit Dystrophin (DMD) ELISA Kit
    abx355333-96tests 96 tests
    EUR 990

    DMD Conjugated Antibody
    C36428 100ul
    EUR 476.4

    anti- DMD antibody
    FNab02423 100µg
    EUR 606.3
    Description: Antibody raised against DMD

    Dystrophin (DMD) Antibody
    20-abx100315
    • EUR 393.60
    • EUR 159.60
    • EUR 944.40
    • EUR 493.20
    • EUR 309.60
    • 100 ug
    • 10 ug
    • 1 mg
    • 200 ug
    • 50 ug

    Dystrophin (DMD) Antibody
    20-abx100316
    • EUR 510.00
    • EUR 159.60
    • EUR 1412.40
    • EUR 693.60
    • EUR 393.60
    • 100 ug
    • 10 ug
    • 1 mg
    • 200 ug
    • 50 ug

    Dystrophin (DMD) Antibody
    20-abx172180
    • EUR 393.60
    • EUR 978.00
    • EUR 510.00
    • EUR 184.80
    • EUR 309.60
    • 100 ug
    • 1 mg
    • 200 ug
    • 20 ug
    • 50 ug

    Dystrophin (DMD) Antibody
    20-abx149852
    • EUR 510.00
    • EUR 410.40
    • 100 ug
    • 50 ug

    Dystrophin (DMD) Antibody
    20-abx112214
    • EUR 878.40
    • EUR 477.60
    • 150 ul
    • 50 ul

    Dystrophin (DMD) Antibody
    20-abx001224
    • EUR 493.20
    • EUR 710.40
    • EUR 218.40
    • EUR 376.80
    • 100 ul
    • 200 ul
    • 20 ul
    • 50 ul

    Dystrophin (DMD) Antibody
    20-abx211560
    • EUR 493.20
    • EUR 360.00
    • 100 ul
    • 50 ul

    Dystrophin (DMD) Antibody
    abx232423-100ug 100 ug
    EUR 577.2

    Dystrophin (DMD) Antibody
    20-abx176215
    • EUR 1412.40
    • EUR 693.60
    • 1 mg
    • 200 ug

    Anti-DMD antibody
    PAab02423 100 ug
    EUR 426

    Anti-DMD antibody
    STJ23394 100 µl
    EUR 332.4
    Description: This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene.

    Anti-DMD antibody
    STJ190175 200 µl
    EUR 236.4
    Description: Unconjugated Rabbit polyclonal to DMD

    Dystrophin Antibody / DMD
    RQ5369 100 ul
    EUR 419

    Dystrophin Antibody / DMD
    V8443-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V8443-20UG 20 ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V8443SAF-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7540-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7540-20UG 20 ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7540IHC-7ML 7 ml
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7540SAF-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7547-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7547-20UG 20 ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7547IHC-7ML 7 ml
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7547SAF-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7548-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7548-20UG 20 ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7548IHC-7ML 7 ml
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7548SAF-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7555-100UG 100 ug
    EUR 499
    Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq]

    Dystrophin Antibody / DMD
    V7555-20UG 20 ug
    EUR 219
    Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq]

    Dystrophin Antibody / DMD
    V7555IHC-7ML 7 ml
    EUR 499
    Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq]

    Dystrophin Antibody / DMD
    V7555SAF-100UG 100 ug
    EUR 499
    Description: The DMD gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [RefSeq]

    Dystrophin Antibody / DMD
    V7561-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7561-20UG 20 ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7561IHC-7ML 7 ml
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7561SAF-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7562-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7562-20UG 20 ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7562IHC-7ML 7 ml
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V7562SAF-100UG 100 ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V8862-100UG 100ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V8862-20UG 20ug
    EUR 219
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V8862SAF-100UG 100ug
    EUR 499
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V4009-100UG 100 ug
    EUR 349.3
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V4009-20UG 20 ug
    EUR 153.3
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin Antibody / DMD
    V4009SAF-100UG 100 ug
    EUR 349.3
    Description: Dystrophin-glycoprotein complex (DGC) connects the F-Actin cytoskeleton on the inner surface of muscle fibers to the surrounding extracellular matrix, through the cell membrane interface. A deficiency in this protein contributes to Duchenne (DMD) and Becker (BMD) muscular dystrophies. The human dystrophin gene measures 2.4 megabases, has more than 80 exons, produces a 14 kb mRNA and contains at least 8 independent tissue-specific promoters and 2 poly A sites. The dystrophin mRNA can undergo differential splicing and produce a range of transcripts that encode a large set of proteins. Dystrophin represents approximately 0.002% of total striated muscle protein and localizes to triadic junctions in skeletal muscle, where it is thought to influence calcium ion homeostasis and force transmission.

    Dystrophin (DMD) Polyclonal Antibody (Human), APC
    4-PAB503Hu01-APC
    • EUR 399.60
    • EUR 3735.60
    • EUR 1046.40
    • EUR 507.60
    • EUR 258.00
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with APC.

    Dystrophin (DMD) Polyclonal Antibody (Human), Biotinylated
    4-PAB503Hu01-Biotin
    • EUR 363.60
    • EUR 2809.20
    • EUR 836.40
    • EUR 442.80
    • EUR 259.20
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with Biotin.

    Dystrophin (DMD) Polyclonal Antibody (Human), Cy3
    4-PAB503Hu01-Cy3
    • EUR 483.60
    • EUR 4930.80
    • EUR 1345.20
    • EUR 627.60
    • EUR 294.00
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with Cy3.

    Dystrophin (DMD) Polyclonal Antibody (Human), FITC
    4-PAB503Hu01-FITC
    • EUR 344.40
    • EUR 3012.00
    • EUR 860.40
    • EUR 430.80
    • EUR 230.40
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with FITC.

    Dystrophin (DMD) Polyclonal Antibody (Human), HRP
    4-PAB503Hu01-HRP
    • EUR 366.00
    • EUR 3256.80
    • EUR 926.40
    • EUR 459.60
    • EUR 243.60
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with HRP.

    Dystrophin (DMD) Polyclonal Antibody (Human), PE
    4-PAB503Hu01-PE
    • EUR 344.40
    • EUR 3012.00
    • EUR 860.40
    • EUR 430.80
    • EUR 230.40
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with PE.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), APC
    4-PAB503Mu01-APC
    • EUR 408.00
    • EUR 3843.60
    • EUR 1072.80
    • EUR 518.40
    • EUR 260.40
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with APC.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), Biotinylated
    4-PAB503Mu01-Biotin
    • EUR 368.40
    • EUR 2888.40
    • EUR 856.80
    • EUR 450.00
    • EUR 260.40
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with Biotin.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), Cy3
    4-PAB503Mu01-Cy3
    • EUR 493.20
    • EUR 5074.80
    • EUR 1381.20
    • EUR 642.00
    • EUR 297.60
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with Cy3.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), FITC
    4-PAB503Mu01-FITC
    • EUR 350.40
    • EUR 3098.40
    • EUR 882.00
    • EUR 439.20
    • EUR 232.80
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with FITC.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), HRP
    4-PAB503Mu01-HRP
    • EUR 373.20
    • EUR 3350.40
    • EUR 949.20
    • EUR 469.20
    • EUR 246.00
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with HRP.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), PE
    4-PAB503Mu01-PE
    • EUR 350.40
    • EUR 3098.40
    • EUR 882.00
    • EUR 439.20
    • EUR 232.80
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with PE.

    DMD siRNA
    20-abx914266
    • EUR 661.20
    • EUR 878.40
    • 15 nmol
    • 30 nmol

    DMD siRNA
    20-abx914267
    • EUR 661.20
    • EUR 878.40
    • 15 nmol
    • 30 nmol

    Dystrophin (DMD) Polyclonal Antibody (Human), APC-Cy7
    4-PAB503Hu01-APC-Cy7
    • EUR 656.40
    • EUR 7327.20
    • EUR 1948.80
    • EUR 872.40
    • EUR 372.00
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Human Dystrophin (DMD). This antibody is labeled with APC-Cy7.

    Dystrophin (DMD) Polyclonal Antibody (Mouse), APC-Cy7
    4-PAB503Mu01-APC-Cy7
    • EUR 672.00
    • EUR 7543.20
    • EUR 2002.80
    • EUR 894.00
    • EUR 378.00
    • 100ul
    • 10ml
    • 1ml
    • 200ul
    • 20ul
    Description: A Rabbit polyclonal antibody against Mouse Dystrophin (DMD). This antibody is labeled with APC-Cy7.

    DMD Antibody, HRP conjugated
    1-CSB-PA006963LB01HU
    • EUR 380.40
    • EUR 402.00
    • 100ug
    • 50ug
    Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is HRP conjugated. Tested in the following application: ELISA

    DMD Rabbit Polyclonal Antibody

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