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EFCAB12 抗体 (AA 421-520) (Biotin)

EFCAB12 适用: 人 ELISA, WB, IHC (p), IHC (fro) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1699910
发货至: 中国
  • 抗原 See all EFCAB12 products
    EFCAB12 (EF-Hand Calcium Binding Domain 12 (EFCAB12))
    抗原表位
    • 14
    • 5
    AA 421-520
    适用
    宿主
    • 19
    克隆类型
    • 19
    多克隆
    标记
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This EFCAB12 antibody is conjugated to Biotin
    应用范围
    • 14
    • 13
    • 13
    • 6
    • 2
    • 2
    • 1
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C3orf25
    亚型
    IgG
  • 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
    EFCAB12 (EF-Hand Calcium Binding Domain 12 (EFCAB12))
    别名
    C3orf25 (EFCAB12 产品)
    别名
    C3orf25 antibody, EF-hand calcium binding domain 12 antibody, EFCAB12 antibody
    背景

    Synonyms: C3orf25, EF-hand domain-containing protein C3orf25, EFC12_HUMAN.

    Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf25 gene product has been provisionally designated C3orf25 pending further characterization.

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