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CPXCR1 抗体 (AA 151-250) (Biotin)

CPXCR1 适用: 人 WB, ELISA, IHC (p), IHC (fro) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1398463
发货至: 中国
  • 抗原 See all CPXCR1 抗体
    CPXCR1 (CPX Chromosome Region, Candidate 1 (CPXCR1))
    抗原表位
    • 14
    • 8
    • 2
    • 1
    AA 151-250
    适用
    • 29
    • 2
    • 1
    • 1
    宿主
    • 26
    • 3
    克隆类型
    • 28
    • 1
    多克隆
    标记
    • 12
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CPXCR1 antibody is conjugated to Biotin
    应用范围
    • 25
    • 13
    • 13
    • 9
    • 4
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    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
    Top Product
    Discover our top product CPXCR1 Primary Antibody
  • 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
    CPXCR1 (CPX Chromosome Region, Candidate 1 (CPXCR1))
    别名
    CPXCR1 (CPXCR1 产品)
    别名
    CT77 antibody, Gm1143 antibody, CPX chromosome region, candidate 1 antibody, CPXCR1 antibody, Cpxcr1 antibody
    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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