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SIM1 抗体 (N-Term)

SIM1 适用: 斑马鱼 WB 宿主: 兔 Polyclonal RB32160 unconjugated
产品编号 ABIN6244173
发货至: 中国
  • 抗原 See all SIM1 抗体
    SIM1 (Single-Minded Homolog 1 (SIM1))
    抗原表位
    • 15
    • 10
    • 4
    • 1
    • 1
    • 1
    AA 1-30, N-Term
    适用
    • 25
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    斑马鱼
    宿主
    • 24
    • 1
    克隆类型
    • 25
    多克隆
    标记
    • 12
    • 3
    • 3
    • 3
    • 2
    • 2
    This SIM1 antibody is un-conjugated
    应用范围
    • 19
    • 17
    • 16
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB)
    预测反应
    M, D
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This Zebrafish SIM1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of Zebrafish SIM1.
    克隆位点
    RB32160
    亚型
    Ig Fraction
    Top Product
    Discover our top product SIM1 Primary Antibody
  • 应用备注
    WB: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    有效期
    6 months
  • 抗原
    SIM1 (Single-Minded Homolog 1 (SIM1))
    别名
    SIM1 (SIM1 产品)
    别名
    bHLHe14 antibody, mSIM1 antibody, single-minded family bHLH transcription factor 1 antibody, single-minded homolog 1 (Drosophila) antibody, single-minded family bHLH transcription factor 1a antibody, SIM1 antibody, Sim1 antibody, sim1a antibody
    背景
    SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.
    分子量
    82919
    UniProt
    F1QMF7
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