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FAM207A 抗体 (AA 95-120)

FAM207A 适用: 人 IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385685
发货至: 中国
  • 抗原 See all FAM207A products
    FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
    抗原表位
    • 14
    • 7
    • 1
    AA 95-120
    适用
    • 23
    • 8
    • 1
    • 1
    • 1
    宿主
    • 23
    克隆类型
    • 23
    多克隆
    标记
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM207A antibody is un-conjugated
    应用范围
    • 12
    • 9
    • 7
    • 6
    • 4
    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 C21orf70
    亚型
    IgG
  • 应用备注
    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
    FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
    别名
    C21orf70 (FAM207A 产品)
    别名
    C21orf70 antibody, 1810008A18Rik antibody, AI303072 antibody, family with sequence similarity 207 member A antibody, family with sequence similarity 207, member A antibody, FAM207A antibody, Fam207a antibody
    背景

    Synonyms: Chromosome 21 open reading frame 70, CU070_HUMAN, Hypothetical protein LOC85395, PRED56, Uncharacterized protein C21orf70.

    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 C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.

    基因ID
    85395
    UniProt
    Q9NSI2
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