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CPXCR1 抗体 (AA 151-250) (Cy3)

This anti-CPXCR1 antibody is a 兔 多克隆 antibody detecting CPXCR1 in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1416329
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for CPXCR1 抗体 (AA 151-250) (Cy3) (ABIN1416329)

抗原

See all CPXCR1 抗体
CPXCR1 (CPX Chromosome Region, Candidate 1 (CPXCR1))

适用

  • 30
  • 2
  • 1
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宿主

  • 27
  • 3

克隆类型

  • 29
  • 1
多克隆

标记

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  • 2
  • 1
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  • 1
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This CPXCR1 antibody is conjugated to Cy3

应用范围

  • 26
  • 12
  • 12
  • 10
  • 5
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  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 8
    • 3
    • 1
    AA 151-250

    预测反应

    Human,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CPXCR1

    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

    CPXCR1 (CPX Chromosome Region, Candidate 1 (CPXCR1))

    别名

    CPXCR1

    背景

    Synonyms: Cancer/testis antigen 77, CPX chromosome region, candidate 1, CPX candidate region 1 protein, CPX chromosomal region candidate gene 1 protein, CPX chromosomal region candidate gene 1 protein homolog, CPX chromosome region, candidate 1, CT77, Gm1143, CPXCR_HUMAN.

    Background: CPXCR1 is widely expressed in fetal tissues, including the tongue, mandible and palate with an unknown function. Cleft palate most commonly occurs as a sporadic multifactorial disorder with a clear but difficult to define genetic component. As a semi-dominant disorder, X-linked cleft palate (CPX) provides a useful model to investigate a congenital defect that is little influenced by non-genetic factors.

    基因ID

    53336
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