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C12orf42 抗体

C12orf42 适用: 人 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385684
发货至: 中国
  • 抗原 See all C12orf42 products
    C12orf42 (Chromosome 12 Open Reading Frame 42 (C12orf42))
    适用
    宿主
    • 17
    克隆类型
    • 17
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
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    • 1
    • 1
    • 1
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    • 1
    • 1
    • 1
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    This C12orf42 antibody is un-conjugated
    应用范围
    • 17
    • 12
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C12ORF42
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    储存方法
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    有效期
    12 months
  • 抗原
    C12orf42 (Chromosome 12 Open Reading Frame 42 (C12orf42))
    别名
    C12ORF42 (C12orf42 产品)
    别名
    chromosome 12 open reading frame 42 antibody, C12orf42 antibody
    背景

    Synonyms: Chromosome 12 open reading frame 42, FLJ25323, Hypothetical protein LOC374470, MGC43592, MGC57409, Uncharacterized protein C12orf42, CL042_HUMAN.

    Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf42 gene product has been provisionally designated C12orf42 pending further characterization.

    基因ID
    374470
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