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WHSC1 抗体

WHSC1 适用: 人, 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263985
发货至: 中国
  • 抗原 See all WHSC1 抗体
    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
    适用
    • 24
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 19
    • 5
    克隆类型
    • 21
    • 3
    多克隆
    标记
    • 14
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WHSC1 antibody is un-conjugated
    应用范围
    • 12
    • 5
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human WHSC1 (NP_579877.1).
    亚型
    IgG
    Top Product
    Discover our top product WHSC1 Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    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 -20°C. Avoid freeze / thaw cycles.
  • 抗原
    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
    别名
    WHSC1 (WHSC1 产品)
    别名
    WHSC1 antibody, fc12c04 antibody, wu:fc12c04 antibody, wu:fi20c01 antibody, si:rp71-77d7.2 antibody, whs antibody, nsd2 antibody, trx5 antibody, mmset antibody, reiibp antibody, MMSET antibody, NSD2 antibody, REIIBP antibody, TRX5 antibody, WHS antibody, RGD1565590 antibody, 5830445G22Rik antibody, 9430010A17Rik antibody, AW555663 antibody, C130020C13Rik antibody, D030027O06Rik antibody, D930023B08Rik antibody, Whsc1l antibody, mKIAA1090 antibody, nuclear receptor binding SET domain protein 2 antibody, Wolf-Hirschhorn syndrome candidate 1 antibody, NSD2 antibody, nsd2 antibody, WHSC1 antibody, Nsd2 antibody
    背景
    This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4,14)(p16.3,q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.
    基因ID
    7468
    UniProt
    O96028
    途径
    SARS-CoV-2 Protein Interactome
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