DMD Rabbit Polyclonal Antibody

DMD Rabbit Polyclonal Antibody

To Order Contact Us Below:

Mouse Dystrophin (DMD) ELISA Kit
RD-DMD-Mu-48Tests	Reddot Biotech	48 Tests	EUR 613.2

Mouse Dystrophin (DMD) ELISA Kit
RD-DMD-Mu-96Tests	Reddot Biotech	96 Tests	EUR 850.8

DMD Polyclonal Antibody
ABP58391-003ml	Abbkine	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	Abbkine	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	Abbkine	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 Polyclonal Antibody
ES9017-100ul	ELK Biotech	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	ELK Biotech	50ul	EUR 248.4
Description: A Rabbit Polyclonal antibody against DMD from Human/Mouse/Rat. This antibody is tested and validated for IHC

DMD Rabbit pAb
A1411-100ul	Abclonal	100 ul	EUR 369.6

DMD Rabbit pAb
A1411-200ul	Abclonal	200 ul	EUR 550.8

DMD Rabbit pAb
A1411-20ul	Abclonal	20 ul	EUR 219.6

DMD Rabbit pAb
A1411-50ul	Abclonal	50 ul	EUR 267.6

Polyclonal DMD / Dystrophin Antibody
APR11762G	Leading Biology	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	Abclonal	96Tests	EUR 625.2

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

DMD Antibody
36428-100ul	SAB	100ul	EUR 302.4

DMD Antibody
1-CSB-PA503789	Cusabio	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	Cusabio	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	Cusabio	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

Dystrophin (DMD) Polyclonal Antibody (Human)
4-PAB503Hu01	Cloud-Clone	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	Cloud-Clone	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	Abbexa	96 tests	EUR 990

Dystrophin (DMD) Polyclonal Antibody (Human), APC
4-PAB503Hu01-APC	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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	Cloud-Clone	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.

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

Dystrophin (DMD) Antibody
20-abx100315	Abbexa	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	Abbexa	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-abx001224	Abbexa	EUR 493.20 EUR 710.40 EUR 218.40 EUR 376.80	100 ul 200 ul 20 ul 50 ul

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

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

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

Dystrophin (DMD) Antibody
20-abx172180	Abbexa	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-abx176215	Abbexa	EUR 1412.40 EUR 693.60	1 mg 200 ug

DMD Conjugated Antibody
C36428	SAB	100ul	EUR 476.4

Anti-DMD antibody
PAab02423	Lifescience Market	100 ug	EUR 426

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

Anti-DMD antibody
STJ190175	St John's Laboratory	200 µl	EUR 236.4
Description: Unconjugated Rabbit polyclonal to DMD

Anti-DMD antibody
STJ23394	St John's Laboratory	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.

Dystrophin Antibody / DMD
V8443-100UG	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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
V7540-100UG	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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	NSJ Bioreagents	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
RQ5369	NSJ Bioreagents	100 ul	EUR 419

Dystrophin (DMD) Polyclonal Antibody (Human), APC-Cy7
4-PAB503Hu01-APC-Cy7	Cloud-Clone	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	Cloud-Clone	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 siRNA
20-abx914266	Abbexa	EUR 661.20 EUR 878.40	15 nmol 30 nmol

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

DMD Antibody, HRP conjugated
1-CSB-PA006963LB01HU	Cusabio	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 Antibody, FITC conjugated
1-CSB-PA006963LC01HU	Cusabio	EUR 380.40 EUR 402.00	100ug 50ug
Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is FITC conjugated. Tested in the following application: ELISA

DMD Antibody, Biotin conjugated
1-CSB-PA006963LD01HU	Cusabio	EUR 380.40 EUR 402.00	100ug 50ug
Description: A polyclonal antibody against DMD. Recognizes DMD from Human. This antibody is Biotin conjugated. Tested in the following application: ELISA

Anti-Dystrophin/DMD Antibody
PB9276	BosterBio	100ug/vial	EUR 400.8

DMD Rabbit Polyclonal Antibody