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TEX43 抗体 (AA 51-134) (Biotin)

This Biotin-conjugated 兔 多克隆 anti-TEX43 antibody specifically detects TEX43 in ELISA, WB, IHC (fro) 和 IHC (p). The antibody is reactive with 人 samples.
产品编号 ABIN1701003
发货至: 中国
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Quick Overview for TEX43 抗体 (AA 51-134) (Biotin) (ABIN1701003)

抗原

TEX43 (Testis expressed 43 (TEX43))

适用

宿主

  • 19
  • 1

克隆类型

  • 19
  • 1
多克隆

标记

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This TEX43 antibody is conjugated to Biotin

应用范围

  • 15
  • 13
  • 13
  • 7
  • 2
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ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 14
    • 6
    AA 51-134

    预测反应

    Human,Mouse,Rat,Dog,Cow,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C5orf48

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    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

    ProClin

    注意事项

    This product contains ProClin: 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 for 12 months.

    有效期

    12 months
  • 抗原

    TEX43 (Testis expressed 43 (TEX43))

    别名

    C5orf48

    背景

    Synonyms: C5orf48, CE048_HUMAN, Chromosome 5 open reading frame 48, Uncharacterized protein C5orf48.

    Background: C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

    基因ID

    389320
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