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TMEM132A 抗体 (PE)

This anti-TMEM132A antibody is a 兔 多克隆 antibody detecting TMEM132A in FACS. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1429565
发货至: 中国

Quick Overview for TMEM132A 抗体 (PE) (ABIN1429565)

抗原

See all TMEM132A 抗体
TMEM132A (Transmembrane Protein 132A (TMEM132A))

适用

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  • 6
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  • 1
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  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 22
  • 1

克隆类型

  • 23
多克隆

标记

  • 9
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TMEM132A antibody is conjugated to PE

应用范围

  • 13
  • 13
  • 7
  • 6
  • 3
  • 3
  • 3
  • 1
  • 1
Flow Cytometry (FACS)
  • 纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human TMEM132A

    亚型

    IgG
  • 应用备注

    FCM(1:20-100)

    说明

    Exitation/Emission: 480,565nm/578nm

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % 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

    -20 °C

    储存方法

    Store at 4°C

    有效期

    12 months
  • 抗原

    TMEM132A (Transmembrane Protein 132A (TMEM132A))

    别名

    Tmem132a

    背景

    TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and â^ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

    Subcellular location: Extracellular


    Synonyms: GBP, HSPA5-binding protein 1, HSPA5BP1, T132A_HUMAN, Tmem132a, Transmembrane protein 132A.
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