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NBPF6 抗体 (C-Term)

NBPF6 适用: 人, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2791688
发货至: 中国
  • 抗原 See all NBPF6 抗体
    NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))
    抗原表位
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    适用
    人, 大鼠
    宿主
    • 12
    克隆类型
    • 12
    多克隆
    标记
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NBPF6 antibody is un-conjugated
    应用范围
    • 5
    • 2
    Western Blotting (WB)
    序列
    STLYSFEDKQ VSLALVDKIK KDQEEIEDQS PPCPRLSQEL PEVKEQEVPE
    预测反应
    Human: 100%, Rat: 75%
    产品特性
    This is a rabbit polyclonal antibody against NBPF6. It was validated on Western Blot.
    纯化方法
    Affinity Purified
    免疫原
    The immunogen is a synthetic peptide directed towards the C-terminal region of Human NBPF6
    Top Product
    Discover our top product NBPF6 Primary Antibody
  • 限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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.
    注意事项
    Avoid repeat freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原
    NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))
    别名
    NBPF6 (NBPF6 产品)
    别名
    NBPF member 6 antibody, NBPF6 antibody
    背景
    This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies.
    Alias Symbols: -
    Protein Size: 667
    分子量
    75 kDa
    基因ID
    653149
    NCBI登录号
    NM_001143987, NP_001137459
    UniProt
    E9PDL3
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