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TMEM67 抗体 (Center)

This anti-TMEM67 antibody is a 兔 多克隆 antibody detecting TMEM67 in WB. Suitable for 人.
产品编号 ABIN2856740
发货至: 中国

Quick Overview for TMEM67 抗体 (Center) (ABIN2856740)

抗原

See all TMEM67 抗体
TMEM67 (Transmembrane Protein 67 (TMEM67))

适用

  • 20
  • 4
  • 2

宿主

  • 21

克隆类型

  • 20
  • 1
多克隆

标记

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TMEM67 antibody is un-conjugated

应用范围

  • 9
  • 6
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Center

    交叉反应

    产品特性

    Rabbit polyclonal antibody to Meckelin (transmembrane protein 67)
    meckelin isoform 1 antibody [N2C1], Internal

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human meckelin isoform 1. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: H1299

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    TMEM67 (Transmembrane Protein 67 (TMEM67))

    别名

    transmembrane protein 67

    背景

    The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).

    Cellular Localization: Cell membrane, Multi-pass membrane protein

    分子量

    112 kDa

    基因ID

    91147

    UniProt

    Q5HYA8
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