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Sarcoglycan, gamma (35kDa Dystrophin-Associated Glycoprotein) (SGCG) Peptide

SGCG 适用: 哺乳动物 宿主: 合成 BP, WB, IHC
产品编号 ABIN938493
发货至: 中国
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Quick Overview for Sarcoglycan, gamma (35kDa Dystrophin-Associated Glycoprotein) (SGCG) Peptide (ABIN938493)

抗原

SGCG (Sarcoglycan, gamma (35kDa Dystrophin-Associated Glycoprotein) (SGCG))

宿主

哺乳动物

资源

  • 3
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • 蛋白类型

    Synthetic

    序列

    FTVDEKEVVV GTDKLRVTGP EGALFEHSVE TPLVRADPFQ DLRLESPTRS

    产品特性

    A synthetic peptide for use as a blocking control in assays to test for specificity of SGCG antibody,
    Alternative Names: SGCG control peptide, SGCG antibody Blocking Peptide, Anti-SGCG Blocking Peptide, Sarcoglycan Gamma Blocking Peptide, 35Kda Dystrophin-Associated Glycoprotein Blocking Peptide, A4 Blocking Peptide, DAGA4 Blocking Peptide, DMDA Blocking Peptide, DMDA1 Blocking Peptide, LGMD2C Blocking Peptide, MAM Blocking Peptide, MGC130048 Blocking Peptide, SCARMD2 Blocking Peptide, SCG3 Blocking Peptide, TYPE Blocking Peptide
  • 应用备注

    Optimal conditions should be determined by the investigator

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    缓冲液

    PBS

    注意事项

    Avoid repeated freeze/thaw cycles.

    储存条件

    -20 °C

    储存方法

    Store at -20 °C long term.
  • 抗原

    SGCG (Sarcoglycan, gamma (35kDa Dystrophin-Associated Glycoprotein) (SGCG))

    背景

    Gamma-sarcoglycan is one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin, probably to provide a link between the membrane associated cytoskeleton and the extracellular matrix. Defects in the protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C).Gamma-sarcoglycan is one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin, probably to provide a link between the membrane associated cytoskeleton and the extracellular matrix. Defects in the protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C).

    分子量

    32 kDa
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