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C21orf62 抗体 (Biotin)

C21orf62 适用: 人, 大鼠, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1405723
发货至: 中国
  • 抗原 See all C21orf62 products
    C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))
    适用
    人, 大鼠, 小鼠
    宿主
    • 16
    • 2
    克隆类型
    • 16
    • 2
    多克隆
    标记
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C21orf62 antibody is conjugated to Biotin
    应用范围
    • 17
    • 13
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C21ORF62
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    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
    C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))
    别名
    C21ORF62 (C21orf62 产品)
    别名
    B37 antibody, PRED81 antibody, C21orf120 antibody, MGC88933 antibody, chromosome 21 open reading frame 62 antibody, chromosome 1 open reading frame, human C21orf62 antibody, chromosome 3 open reading frame, human C21orf62 antibody, C21orf62 antibody, C1H21ORF62 antibody, c21orf62 antibody, C3H21orf62 antibody
    背景

    Synonyms: B37, C21orf120, Chromosome 21 open reading frame 62, Hypothetical protein LOC56245, PRED81, Uncharacterized protein C21orf62, CU062_HUMAN.

    Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.

    基因ID
    56245
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