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GPATCH4 抗体 (AA 236-262)

The 兔 多克隆 anti-GPATCH4 antibody (Clone RB37527) (ABIN1538148) specifically detects GPATCH4 in WB. The antibody is reactive with 人 samples.
产品编号 ABIN1538148
发货至: 中国
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Quick Overview for GPATCH4 抗体 (AA 236-262) (ABIN1538148)

抗原

See all GPATCH4 抗体
GPATCH4 (G Patch Domain Containing 4 (GPATCH4))

适用

  • 15
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1

宿主

  • 13
  • 2

克隆类型

  • 15
多克隆

标记

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
This GPATCH4 antibody is un-conjugated

应用范围

  • 15
  • 8
  • 1
  • 1
Western Blotting (WB)

克隆位点

RB37527
  • 抗原表位

    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 236-262

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This GPATCH4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 236-262 amino acids from the Central region of human GPATCH4.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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.

    储存条件

    4 °C,-20 °C

    储存方法

    GPATCH4 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    有效期

    6 months
  • 抗原

    GPATCH4 (G Patch Domain Containing 4 (GPATCH4))

    别名

    GPATCH4

    背景

    GPATCH4 (G patch domain-containing protein 4) is a 446 amino acid protein containing one G-patch domain. Existing as three alternatively spliced isoforms, the gene encoding GPATCH4 maps to human chromosome 1q23.1 and mouse chromosome 3 F1. Spanning around 260 million base pairs, chromosome 1 is the largest human chromosome and comprises 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    分子量

    50381

    基因ID

    54865

    UniProt

    Q5T3I0
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