Dystrophin Polyclonal Antibody | Invitrogen PA5-16734 product information

This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.

product summary

company name :

Invitrogen

other brands :

NeoMarkers, Lab Vision, Endogen, Pierce, BioSource International, Zymed Laboratories, Caltag, Molecular Probes, Research Genetics, Life Technologies, Applied Biosystems, GIBCO BRL, ABgene, Dynal, Affinity BioReagents, Nunc, Invitrogen, NatuTec, Oxoid, Richard-Allan Scientific, Arcturus, Perseptive Biosystems, Proxeon, eBioscience

product type :

antibody

product name :

Dystrophin Polyclonal Antibody

catalog :

PA5-16734

quantity :

500 µL

price :

US 436.00

clonality :

polyclonal

host :

domestic rabbit

conjugate :

nonconjugated

reactivity :

human, mouse, rat

application :

immunohistochemistry, immunohistochemistry - paraffin section

citations: 8

Published Application/Species/Sample/Dilution	Reference
immunohistochemistry; mouse; fig 1	Ryan T, Schmidt C, Green T, Spangenburg E, Neufer P, McClung J. Targeted Expression of Catalase to Mitochondria Protects Against Ischemic Myopathy in High-Fat Diet-Fed Mice. Diabetes. 2016;65:2553-68 pubmed publisher
	Wellmann K, Kim J, Urso P, Smith Z, Johnson B. Evaluation of vitamin A status on myogenic gene expression and muscle fiber characteristics. J Anim Sci. 2021;99: pubmed publisher
	Iyer S, Xu S, Shah S, Lovering R. Muscle phenotype of a rat model of Duchenne muscular dystrophy. Muscle Nerve. 2020;62:757-761 pubmed publisher
	Klimczak A, Zimna A, Malcher A, Kozlowska U, Futoma K, Czarnota J, et al. Co-Transplantation of Bone Marrow-MSCs and Myogenic Stem/Progenitor Cells from Adult Donors Improves Muscle Function of Patients with Duchenne Muscular Dystrophy. Cells. 2020;9: pubmed publisher
	Lee J. A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report. Ann Indian Acad Neurol. 2020;23:123-125 pubmed publisher
	Romero M, Mobley C, Mumford P, Roberson P, Haun C, Kephart W, et al. Acute and chronic resistance training downregulates select LINE-1 retrotransposon activity markers in human skeletal muscle. Am J Physiol Cell Physiol. 2018;314:C379-C388 pubmed publisher
	Vulin A, Wein N, Simmons T, Rutherford A, Findlay A, Yurkoski J, et al. The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development. Neuromuscul Disord. 2015;25:827-34 pubmed publisher
	Pratt S, Shah S, Ward C, Kerr J, Stains J, Lovering R. Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury. Cell Mol Life Sci. 2015;72:153-64 pubmed publisher

product information

Product Type :

Antibody

Product Name :

Dystrophin Polyclonal Antibody

Catalog # :

PA5-16734

Quantity :

500 µL

Price :

US 436.00

Clonality :

Polyclonal

Purity :

purified

Host :

Rabbit

Reactivity :

Human, Rat

Applications :

Immunohistochemistry (Paraffin): 1:200-1:400

Species :

Human, Rat

Isotype :

IgG

Storage :

4° C

Description :

Dystrophin is the 427kDa protein product of the DMB/BMD gene located on the X chromosome at position Xp21. Western blotting and immunohistochemistry are the two established methods for the detection of abnormalities of dystrophin expression in muscle biopsies. Dystrophin abnormalities are thought to occur in 100% of patients with DMD/BMD, although genetic abnormalities may only be detected in up to 65% of cases.

Immunogen :

A synthetic peptide corresponding to C-terminal of human Dystrophin

Format :

Liquid

Applications w/Dilutions :

Immunohistochemistry (Paraffin): 1:200-1:400

Aliases :

apodystrophin-3; apodystrophin-I; BMD; CMD3B; dmd; dmd.1; dmd.1.L; DNADMD1; Dp427; Dp71; Duchenne muscular dystrophy (DMD); DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; DXSmh7; DXSmh9; dys; Dystrophin; dystrophin Dp40; dystrophin Dp71 isoform; dystrophin Dp71a; dystrophin Dp71ab; dystrophin Dp71b; dystrophin, gene 1 L homeolog; dystrophin, muscular dystrophy; GS1-19O24.1; mdx; MRX85; Muscular dystrophy Duchenne and Becker types; OTTHUMP00000215592; pke; utrn; utrophin; XELAEV_18012903mg; X-linked muscular dystrophy