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NBPF4 抗体 (AA 48-97)

The 兔 多克隆 anti-NBPF4 antibody (ABIN1451391) specifically detects NBPF4 in IHC, ELISA 和 IF. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN1451391
发货至: 中国
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Quick Overview for NBPF4 抗体 (AA 48-97) (ABIN1451391)

抗原

See all NBPF4 抗体
NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))

适用

人, 小鼠, 大鼠

宿主

  • 3
兔

克隆类型

  • 3
多克隆

标记

  • 3
This NBPF4 antibody is un-conjugated

应用范围

  • 3
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • 抗原表位

    • 1
    • 1
    • 1
    AA 48-97

    原理

    NBPF4 Antibody

    特异性

    NBPF4 Polyclonal Antibody detects endogenous levels of NBPF4 protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    纯度

    > 95 %

    免疫原

    The antiserum was produced against synthesized peptide derived from human NBPF4. AA range:48-97

    亚型

    IgG
  • 应用备注

    IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

    NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))

    别名

    NBPF4

    背景

    Synonyms: NBPF4, Neuroblastoma breakpoint family member 4

    Background: neuroblastoma breakpoint family member 4(NBPF4) Homo sapiens 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. Altered expression of some gene family members is associated with several types of cancer. This gene fam

    Gene Name: NBPF4

    Protein Name: Neuroblastoma breakpoint family member 4

    分子量

    14 kDa

    基因ID

    148545

    UniProt

    Q96M43
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