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GLYATL1 抗体 (AA 101-200) (Cy5.5)

This anti-GLYATL1 antibody is a 兔 多克隆 antibody detecting GLYATL1 in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1705445
发货至: 中国

Quick Overview for GLYATL1 抗体 (AA 101-200) (Cy5.5) (ABIN1705445)

抗原

See all GLYATL1 抗体
GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))

适用

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宿主

  • 22
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克隆类型

  • 23
多克隆

标记

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This GLYATL1 antibody is conjugated to Cy5.5

应用范围

  • 23
  • 12
  • 12
  • 7
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  • 5
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 3
    • 2
    • 1
    AA 101-200

    交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GLYATL1

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

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

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))

    别名

    GLYATL1

    背景

    Synonyms: Acyl CoA glycine N acyltransferase like protein 1, EC 2.3.1.13, FLJ26507, FLJ34646, GATF C, GATFC, Glycine N acyltransferase like 1, GNAT, MGC15397, MGC15937, GLYL1_HUMAN.

    Background: GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

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