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GIDRP88 抗体

C10orf28 适用: 人, 小鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7243328
发货至: 中国
  • 抗原 See all GIDRP88 (C10orf28) products
    GIDRP88 (C10orf28) (Chromosome 10 Open Reading Frame 28 (C10orf28))
    适用
    • 27
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    人, 小鼠
    宿主
    • 27
    克隆类型
    • 27
    多克隆
    标记
    • 6
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    • 1
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    This GIDRP88 antibody is un-conjugated
    应用范围
    • 20
    • 13
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    • 7
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    • 3
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human R3HCC1L
    亚型
    IgG
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.7 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    GIDRP88 (C10orf28) (Chromosome 10 Open Reading Frame 28 (C10orf28))
    别名
    R3HCC1L (C10orf28 产品)
    别名
    1700036B12Rik antibody, AI450607 antibody, C10orf28 antibody, D19Ertd386e antibody, GIDRP86 antibody, Gidrp88 antibody, GIDRP88 antibody, PSORT antibody, R3H domain and coiled-coil containing 1 like antibody, R3hcc1l antibody, R3HCC1L antibody
    背景
    C10orf28 (chromosome 10 open reading frame 28), also known as GIDRP88 (growth inhibition and differentiation-related protein 88) or putative mitochondrial space protein 32.1, is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
    NCBI登录号
    NP_001243548
    UniProt
    Q7Z5L2
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