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DGCR14 抗体

DGCR14 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6290316
发货至: 中国
  • 抗原 See all DGCR14 抗体
    DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))
    适用
    • 21
    • 3
    • 2
    人, 小鼠
    宿主
    • 20
    • 1
    克隆类型
    • 21
    多克隆
    标记
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    This DGCR14 antibody is un-conjugated
    应用范围
    • 21
    • 15
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant Protein of human DGCR14
    亚型
    IgG
    Top Product
    Discover our top product DGCR14 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    说明

    Highly expressed in heart, brain and skeletal muscle, Detected at low levels in placenta

    限制
    仅限研究用
  • 缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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 -20C. Avoid freeze / thaw cycles.
  • 抗原
    DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))
    别名
    DGCR14 (DGCR14 产品)
    别名
    DGCR13 antibody, DGS-H antibody, DGS-I antibody, DGSH antibody, DGSI antibody, ES2 antibody, Es2el antibody, AI462402 antibody, D16H22S1269E antibody, Dgcr1 antibody, Dgsi antibody, fc19d10 antibody, wu:fc19d10 antibody, zgc:162979 antibody, MGC82189 antibody, DGCR14 antibody, es2 antibody, dgsi antibody, dgs-h antibody, dgs-i antibody, es2el antibody, dgcr13 antibody, ess-2 splicing factor homolog antibody, DiGeorge syndrome critical region gene 14 antibody, ess-2 splicing factor homolog S homeolog antibody, ESS2 antibody, Dgcr14 antibody, ess2 antibody, Ess2 antibody, DGCR14 antibody, ess2.S antibody
    背景
    This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene.
    分子量
    52.568 kDa
    基因ID
    8220
    UniProt
    Q96DF8
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