NBPF5 Polyclonal Antibody
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  • NBPF5 Polyclonal Antibody

NBPF5 Polyclonal Antibody


货       号:

YM-A19292

规       格:

50μL;100μL

种属反应:

Human

实验应用:

WB,IHC,IF,ELISA

说明书:

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产品详情


产品名称

NBPF5 Polyclonal Antibody

产品货号

YM-A19292

规格

50μL;100μL

种属反应

Human

实验应用

WB,IHC,IF,ELISA

分子量

41kD

宿主

Rabbit

同种型

IgG

修饰

Unmodified

推荐稀释比

WB 1:500-1:2000;IHC 1:100-1:300;ELISA 1:10000;IF 1:50-200

组成

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

纯化工艺

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

储存

-15°C to -25°C/1 year(Do not lower than -25°C)

浓度

1 mg/ml

克降性

Polyclonal

克隆号

免疫原

The antiserum was produced against synthesized peptide derived from human NBPF5. AA range:302-351

特异性

NBPF5 Polyclonal Antibody detects endogenous levels of NBPF5 protein.

基因名称

NBPF5

蛋白名称

Neuroblastoma breakpoint family member 5

别名

NBPF5;Neuroblastoma breakpoint family member 5

基因ID-1

284610

SwissProt

Q86XG9

背景

NBPF5 (neuroblastoma breakpoint family member 5) is a 351 amino acid cytoplasmic protein that is expressed in medulla and brain and belongs to the NBPF family. NBPF5 contains one NBPF domain and is encoded by a gene that maps to human chromosome 1p13. Chromosome 1 spans 260 million base pairs, contains over 3000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

细胞定位

Cytoplasm .

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