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EFHA1 抗体 (PE)

This anti-EFHA1 antibody is a 兔 多克隆 antibody detecting EFHA1 in WB. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN2173807
发货至: 中国

Quick Overview for EFHA1 抗体 (PE) (ABIN2173807)

抗原

See all EFHA1 抗体
EFHA1 (EF-Hand Domain Family, Member A1 (EFHA1))

适用

人, 小鼠, 大鼠

宿主

  • 22
  • 2

克隆类型

  • 24
多克隆

标记

  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EFHA1 antibody is conjugated to PE

应用范围

  • 18
  • 13
  • 5
  • 3
  • 1
Western Blotting (WB)
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human EFHA1

    亚型

    IgG
  • 应用备注

    FCM: (1:20-100)
    Optimal working dilution should be determined by the investigator.

    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

    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

    -20 °C

    储存方法

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

    EFHA1 (EF-Hand Domain Family, Member A1 (EFHA1))

    别名

    EFHA1

    背景

    Synonyms: EF-HA1, EF hand domain containing family member A1, EF hand domain family A1, EF hand domain family member A1, EFHA1 EF hand domain family member A1, FLJ25016, FLJ34588, Smhs2 homolog, 1110008L20Rik, EFHA1_HUMAN.

    Background: The EF-hand domain is a twelve amino acid loop motif that is commonly found in proteins that participate in calcium-binding events within the cell. EF-hand domains generally exist in a pair that, together, form a stable four-helix bundle that enables the binding of calcium ions. EF-HA1 (EF-hand domain family, member A1) is a 434 amino acid protein that contains four EF-hand domains, suggesting a role in calcium-mediated events throughout the cell. The gene encoding EF-HA1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4 % of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.

    基因ID

    221154
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