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C6ORF1 抗体 (FITC)

This anti-C6ORF1 antibody is a 兔 多克隆 antibody detecting C6ORF1 in WB 和 IF (p). Suitable for 人.
产品编号 ABIN1403276
发货至: 中国

Quick Overview for C6ORF1 抗体 (FITC) (ABIN1403276)

抗原

C6ORF1 (Chromosome 6 Open Reading Frame 1 (C6ORF1))

适用

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宿主

  • 16

克隆类型

  • 16
多克隆

标记

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This C6ORF1 antibody is conjugated to FITC

应用范围

  • 16
  • 12
  • 3
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C6orf1

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200

    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    C6ORF1 (Chromosome 6 Open Reading Frame 1 (C6ORF1))

    别名

    C6orf1

    背景

    Synonyms: C6orf1, CF001_HUMAN, Chromosome 6 open reading frame 1, Hypothetical protein LOC221491, LBH, MGC57858, Protein LBH, Uncharacterized protein C6orf1.

    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 C6orf1 gene product has been provisionally designated C6orf1 pending further characterization.

    基因ID

    221491
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