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CXorf56 抗体 (AA 120-170) (Biotin)

CXORF56 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1403371
发货至: 中国
  • 抗原 See all CXorf56 (CXORF56) 抗体
    CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
    抗原表位
    • 14
    • 5
    • 1
    AA 120-170
    适用
    • 21
    • 16
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 21
    克隆类型
    • 21
    多克隆
    标记
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CXorf56 antibody is conjugated to Biotin
    应用范围
    • 16
    • 13
    • 5
    • 2
    • 1
    • 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 CXorf56
    亚型
    IgG
    Top Product
    Discover our top product CXORF56 Primary Antibody
  • 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
    CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
    别名
    CXorf56 (CXORF56 产品)
    别名
    C4HXorf56 antibody, CXorf56 antibody, c330007p06-a antibody, cxorf56 antibody, chromosome X open reading frame 56 antibody, chromosome 4 CXorf56 homolog antibody, chromosome X open reading frame, human CXorf56 antibody, RIKEN cDNA C330007P06 gene antibody, chromosome X open reading frame 56 L homeolog antibody, CXorf56 antibody, C4HXorf56 antibody, CXHXorf56 antibody, C330007P06Rik antibody, cxorf56.L antibody
    背景

    Synonyms: UPF0428 protein CXorf56, CXorf56

    Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.

    基因ID
    63932
    UniProt
    Q9H5V9
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