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C3orf65 抗体 (AA 1-100) (Biotin)

C3ORF65 适用: 人 WB, ELISA, IHC (fro), IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1699914
发货至: 中国
  • 抗原 See all C3orf65 (C3ORF65) products
    C3orf65 (C3ORF65) (Chromosome 3 Open Reading Frame 65 (C3ORF65))
    抗原表位
    AA 1-100
    适用
    宿主
    • 14
    克隆类型
    • 14
    多克隆
    标记
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C3orf65 antibody is conjugated to Biotin
    应用范围
    • 14
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    Human
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C3orf65
    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
    C3orf65 (C3ORF65) (Chromosome 3 Open Reading Frame 65 (C3ORF65))
    别名
    C3orf65 (C3ORF65 产品)
    别名
    IGF2BP2 antisense RNA 1 antibody, IGF2BP2-AS1 antibody
    背景

    Synonyms: Chromosome 3 open reading frame 65, FLJ32900, CC065_HUMAN.

    Background: C3orf65 (chromosome 3 open reading frame 65) is a 143 amino acid protein encoded by a gene that maps to human chromosome 3q27.2. Chromosome 3 is made up of approximately 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.

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