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C10orf62 抗体 (PE)

This anti-C10orf62 antibody (ABIN1437542) is a Rabbit Polyclonal antibody detecting C10orf62 in WB. Suitable for Human, Mouse, Rat.
产品编号 ABIN1437542
发货至: 中国

Quick Overview for C10orf62 抗体 (PE) (ABIN1437542)

抗原

C10orf62 (C10ORF62) (Chromosome 10 Open Reading Frame 62 (C10ORF62))

适用

  • 22
  • 18
  • 18
  • 3
人, 小鼠, 大鼠

宿主

  • 22

克隆类型

  • 22
多克隆

标记

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This C10orf62 antibody is conjugated to PE

应用范围

  • 18
  • 13
  • 4
  • 3
  • 1
Western Blotting (WB)
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C10orf62

    亚型

    IgG
  • 应用备注

    FCM: (1:20-100)
    Optimal working dilution should be determined by the investigator.

    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

    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 -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    C10orf62 (C10ORF62) (Chromosome 10 Open Reading Frame 62 (C10ORF62))

    别名

    C10orf62

    背景

    Synonyms: bA548K23.1, Hypothetical protein LOC414157, MERIT40, chromosome 10 open reading frame 62, NBA1, Uncharacterized protein C10orf62, CJ062_HUMAN .

    Background: C10orf62 is a 223 amino acid protein encoded by a gene that maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

    基因ID

    414157
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