NBPF4 抗体 (AA 20-100)
This anti-NBPF4 antibody is a 兔 多克隆 antibody detecting NBPF4 in ELISA 和 IHC (p). Suitable for 人.
Quick Overview for NBPF4 抗体 (AA 20-100) (ABIN7219800)
抗原
See all NBPF4 抗体
NBPF4
(Neuroblastoma Breakpoint Family, Member 4 (NBPF4))
适用
人
宿主
兔
克隆类型
多克隆
标记
This NBPF4 antibody is un-conjugated
应用范围
ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
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抗原表位
- AA 20-100
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原理
- NBPF4 Polyclonal Antibody
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特异性
- NBPF4 Polyclonal Antibody detects endogenous levels of NBPF4 protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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免疫原
- Synthesized peptide derived from the Internal region of human NBPF4 at AA range: 20-100
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亚型
- IgG
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anti-Neuroblastoma Breakpoint Family, Member 4 (NBPF4) antibody
NBPF4 适用: 人, 小鼠 ELISA, IHC, WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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说明
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Primary Antibody
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))
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别名
- NBPF4
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背景
- Rabbit Anti-NBPF4 Polyclonal Antibody,NBPF4, Neuroblastoma breakpoint family member 4,NBPF4 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. , 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 family contains numerous pseudogenes.,Neuroblastoma breakpoint family member 4
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基因ID
- 148545
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UniProt
- Q96M43
抗原
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