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Mannosyl (Alpha-1,6-)-Glycoprotein beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Peptide

MGAT2 适用: 哺乳动物 宿主: 合成 BP, WB, IHC
产品编号 ABIN936004
发货至: 中国

Quick Overview for Mannosyl (Alpha-1,6-)-Glycoprotein beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Peptide (ABIN936004)

抗原

MGAT2 (Mannosyl (Alpha-1,6-)-Glycoprotein beta-1,2-N-Acetylglucosaminyltransferase (MGAT2))

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

    YAGLILFLEE DHYLAPDFYH VFKKMWKLKQ QECPECDVLS LGTYSASRSF

    产品特性

    A synthetic peptide for use as a blocking control in assays to test for specificity of MGAT2 antibody,
    Alternative Names: MGAT2 control peptide, MGAT2 antibody Blocking Peptide, Anti-MGAT2 Blocking Peptide, Mannosyl Blocking Peptide, Alpha 1-6-Glycoprotein Beta-1-2-N-Acetylglucosaminyltransferase Blocking Peptide, CDGS2 Blocking Peptide, GLCNACTII Blocking Peptide, GNT-II Blocking Peptide, GNT2 Blocking Peptide, MGAT2, MGAT-2, MGAT 2, MGAT-2 Blocking Peptide, MGAT 2 Blocking Peptide

    纯化方法

    The antibody is affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide is removed by chromatogramphy using non-phosphopeptide corresponding to the phosphorylation site.
  • 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

    MGAT2 (Mannosyl (Alpha-1,6-)-Glycoprotein beta-1,2-N-Acetylglucosaminyltransferase (MGAT2))

    背景

    MGAT2 is a Golgi enzyme catalyzing an essential step in the conversion of oligomannose to complex N-glycans. The enzyme has the typical glycosyltransferase domains: a short N-terminal cytoplasmic domain, a hydrophobic non-cleavable signal-anchor domain, and a C-terminal catalytic domain. Mutations in its gene may lead to carbohydrate-deficient glycoprotein syndrome, type II. The product of this gene is a Golgi enzyme catalyzing an essential step in the conversion of oligomannose to complex N-glycans.

    分子量

    51 kDa
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