discontinued

AP26166PU-N Myospryn (C-term) antibody

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Rabbit anti Human, Mouse, Rat Myospryn

AP26166PU-N

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  • AP26166PU-N
  • AP26166PU-N

Product Description for Myospryn

Rabbit anti Human, Mouse, Rat Myospryn.
Properties: (C-term)
Presentation: Aff - Purified
Product is tested for Enzyme Immunoassay, Western blot / Immunoblot.

Properties for Myospryn

Product Category Primary Antibodies
Target Category
Quantity 0.1 mg
Synonyms C5orf10, CMYA5, Cardiomyopathy-associated protein 5, DTNBP2, Dystrobrevin-binding protein 2, Genethonin-3, SPRY domain-containing protein 2, SPRYD2, TRIM76, Tripartite motif-containing protein 76
Presentation Aff - Purified
Reactivity Hu, Ms, Rt
Applications E, WB
Clonality Polyclonal
Host Rabbit
Shipping to Worldwide
PDF datasheet View Datasheet
Manufacturer OriGene Technologies GmbH
Material safety datasheet MSDS for Polyclonal Antibodies (de)

Datasheet Extract

Immunogen
Swiss Prot Num:
Q8N3K9
Immunogen:
18 amino acid peptide near the carboxy terminus of human SPRYD2
GeneID:
202333
Property C-term
Application ELISA.
Western blot: 1-2 µg/ml.
Positive control: Rat Brain Tissue Lysate.
Background SPRYD2, also known as Myospryn, was originally identified as the muscle-specific partner of dysbindin and as a Mef-2 target gene. It is a large scaffolding protein localized to the Z-disc/costamere region of striated muscle. SPRYD2 includes a noncanonical tripartite motif (TRIM-like) that lacks the RING domain but consists of a B-box coiled coil (BBC), fibronectin 3 (FN3) repeats, and SPRY domains. SPRYD2 interacts with desmin and calcineurin, and it has been suggested to play a role in the biogenesis of lysosome and negatively regulates slow-fiber-type transformation and skeletal muscle regeneration. SPRYD2 is dysregulated in Duchenne muscular dystrophy.
General Readings
  1. Benson MA, Tinsley CL, Blake DJ. Myospryn is a novel binding partner for dysbindin in muscle. J Biol Chem. 2004 Mar 12;279(11):10450-8. Epub 2003 Dec 19. PubMed PMID: 14688250.
  2. Sarparanta J. Biology of myospryn: what's known? J. Muscle Res. Cell Motil. 2008; 29:177-80
  3. Durham JT, Brand OM, Arnold M, Reynolds JG, Muthukumar L, Weiler H, et al. Myospryn is a direct transcriptional target for MEF2A that encodes a striated muscle, alpha-actinin-interacting, costamere-localized protein. J Biol Chem. 2006 Mar 10;281(10):6841-9. Epub 2006 Jan 3. PubMed PMID: 16407236.
  4. Kielbasa OM, Reynolds JG, Wu CL, Snyder CM, Cho MY, Weiler H, et al. Myospryn is a calcineurin-interacting protein that negatively modulates slow-fiber-type transformation and skeletal muscle regeneration. FASEB J. 2011 Jul;25(7):2276-86. doi: 10.1096/fj.10-169219. Epub 2011 Mar 22. PubMed PMID: 21427212. (Free PMC Article available, 5 images available)
Storage Store at 2 - 8 °C for up to three months or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing.
Shelf life: one year from despatch.
Format
Purification:
Affinity chromatography purified via peptide column
Buffer System:
PBS containing 0.02% sodium azide
State:
Liquid Ig fraction
Aff - Purified
Species Reactivity
Species reactivity (tested):
Human, mouse, rat.
Specificity
Specificity:
This antibody detects Myospryn at C-term.
SPRYD2 antibody is predicted to not cross-react with other SPRYD protein family members. At least four isoforms of SPRYD2 are known to exist.
Gene ID 202333

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