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C6ORF52 抗体 (AA 1-100) (Biotin)

This anti-C6ORF52 antibody is a 兔 多克隆 antibody detecting C6ORF52 in WB, ELISA, IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN1699926
发货至: 中国

Quick Overview for C6ORF52 抗体 (AA 1-100) (Biotin) (ABIN1699926)

抗原

C6ORF52 (Chromosome 6 Open Reading Frame 52 (C6ORF52))

适用

宿主

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克隆类型

  • 14
多克隆

标记

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This C6ORF52 antibody is conjugated to Biotin

应用范围

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

    AA 1-100

    交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C6orf52

    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

    C6ORF52 (Chromosome 6 Open Reading Frame 52 (C6ORF52))

    别名

    C6orf52

    背景

    Synonyms: chromosome 6 open reading frame 52, putative uncharacterized protein C6orf52,CF052_HUMAN.

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf52 gene product has been provisionally designated C6orf52 pending further characterization.

    基因ID

    347744
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