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NBPF6 抗体 (N-Term)

This anti-NBPF6 antibody is a 兔 多克隆 antibody detecting NBPF6 in WB. Suitable for 人.
产品编号 ABIN2791691
发货至: 中国

Quick Overview for NBPF6 抗体 (N-Term) (ABIN2791691)

抗原

See all NBPF6 抗体
NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))

适用

  • 5
  • 1

宿主

  • 5

克隆类型

  • 5
多克隆

标记

  • 5
This NBPF6 antibody is un-conjugated

应用范围

  • 5
  • 2
Western Blotting (WB)
  • 抗原表位

    • 2
    • 1
    • 1
    • 1
    N-Term

    序列

    EKVQESPAPR EVQKTEEKEV PQDSLEECAV TCSNSHNPSN SNQPHRSTKI

    预测反应

    Human: 100%

    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 N-terminal region of Human NBPF6
  • 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

    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: 638

    分子量

    70 kDa

    基因ID

    653149

    NCBI登录号

    NM_001143988, NP_001137460

    UniProt

    Q5VWK0
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