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GJC2 抗体 (Middle Region)

This anti-GJC2 antibody is a 兔 多克隆 antibody detecting GJC2 in WB 和 IHC. Suitable for 人 和 兔.
产品编号 ABIN2774865
发货至: 中国

Quick Overview for GJC2 抗体 (Middle Region) (ABIN2774865)

抗原

See all GJC2 抗体
GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))

适用

  • 19
  • 12
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  • 1
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人, 兔

宿主

  • 16
  • 6

克隆类型

  • 16
  • 6
多克隆

标记

  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This GJC2 antibody is un-conjugated

应用范围

  • 15
  • 5
  • 4
  • 3
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  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    序列

    APASRTGSAT SAGTVGEQGR PGTHERPGAK PRAGSEKGSA SSRDGKTTVW

    预测反应

    Human: 100%, Rabbit: 100%

    产品特性

    This is a rabbit polyclonal antibody against GJC2. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human GJC2
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 439 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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 freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))

    别名

    GJC2

    背景

    GJC2 is a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.
    Alias Symbols: CX46.6, Cx47, GJA12, MGC105119, PMLDAR, HLD2, SPG44, LMPH1C
    Protein Interaction Partner: ALB,
    Protein Size: 439

    分子量

    47 kDa

    基因ID

    57165

    NCBI登录号

    NM_020435, NP_065168

    UniProt

    Q5T442
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