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CMYA5 抗体 (C-Term)

The 兔 多克隆 anti-CMYA5 antibody (ABIN783522) specifically detects CMYA5 in WB 和 EIA. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN783522
发货至: 中国
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Quick Overview for CMYA5 抗体 (C-Term) (ABIN783522)

抗原

CMYA5 (Cardiomyopathy Associated 5 (CMYA5))

适用

人, 小鼠, 大鼠

宿主

  • 1

克隆类型

  • 1
多克隆

标记

  • 1
This CMYA5 antibody is un-conjugated

应用范围

  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • 抗原表位

    • 1
    • 1
    C-Term

    特异性

    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.

    交叉反应 (详细)

    Species reactivity (tested):Human, mouse, rat.

    纯化方法

    Affinity chromatography purified via peptide column

    免疫原

    18 amino acid peptide near the carboxy terminus of human SPRYD2
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 缓冲液

    PBS containing 0.02 % sodium azide

    储存液

    Sodium azide

    注意事项

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store at 2 - 8 °C for up to three months or (in aliquots) at -20 °C for longer.
  • 抗原

    CMYA5 (Cardiomyopathy Associated 5 (CMYA5))

    别名

    Myospryn

    背景

    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.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

    基因ID

    202333

    NCBI登录号

    NP_705838

    UniProt

    Q8N3K9
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