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FAM203B 抗体

FAM203B 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7244606
发货至: 中国
  • 抗原 See all FAM203B products
    FAM203B (Family with Sequence Similarity 203, Member B (FAM203B))
    适用
    • 40
    • 13
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    宿主
    • 38
    • 2
    克隆类型
    • 40
    多克隆
    标记
    • 16
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM203B antibody is un-conjugated
    应用范围
    • 40
    • 20
    • 13
    • 13
    • 5
    • 4
    • 3
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human HGH1
    亚型
    IgG
  • 应用备注
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.6 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
  • 抗原
    FAM203B (Family with Sequence Similarity 203, Member B (FAM203B))
    别名
    HGH1 (FAM203B 产品)
    别名
    Brp16 antibody, D15Ertd741e antibody, brp16 antibody, zgc:92803 antibody, c8orf30b antibody, fam203b antibody, BRP16 antibody, C8orf30A antibody, HGH1 homolog antibody, HGH1 homolog (S. cerevisiae) antibody, HGH1 homolog L homeolog antibody, Hgh1 antibody, hgh1 antibody, hgh1.L antibody, HGH1 antibody
    背景
    HGH1, is also known as BRP16, Brp16 is a 256 amino acid protein encoded by a gene on human chromosome 8. Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
    UniProt
    Q9BTY7
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