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C22orf13 抗体 (AA 51-150) (FITC)

This FITC-conjugated 兔 多克隆 anti-C22orf13 antibody specifically detects C22orf13 in WB, IF (cc) 和 IF (p). The antibody is reactive with 人 samples.
产品编号 ABIN1710125
发货至: 中国
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Quick Overview for C22orf13 抗体 (AA 51-150) (FITC) (ABIN1710125)

抗原

C22orf13 (GUCD1) (Guanylyl Cyclase Domain Containing 1 (GUCD1))

适用

  • 23
  • 3
  • 3
  • 2
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  • 1

宿主

  • 23

克隆类型

  • 23
多克隆

标记

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  • 2
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  • 1
  • 1
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This C22orf13 antibody is conjugated to FITC

应用范围

  • 19
  • 12
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  • 8
  • 3
  • 3
  • 2
  • 1
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 6
    • 1
    • 1
    • 1
    AA 51-150

    交叉反应

    预测反应

    Mouse,Rat,Dog,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C22orf13

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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

    C22orf13 (GUCD1) (Guanylyl Cyclase Domain Containing 1 (GUCD1))

    别名

    C22orf13

    背景

    Synonyms: C22orf13, CG13760 gene product [Drosophila melanogaster] homolog, Chromosome 22 open reading frame 13, CV013_HUMAN, LLN4, MGC1842, OTTHUMP00000198388, Protein LLN4, Uncharacterized protein C22orf13.

    Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.

    基因ID

    83606
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