兔抗NBPF5多克隆抗体

Background:

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 1p13.3. Chromosome 1 spans 260 million base pairs, contains over 3,000 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.

Applications:

WB

Name of antibody:

NBPF5

Immunogen:

Synthesized peptide derived from C-terminal of human NBPF5.

Full name:

neuroblastoma breakpoint family, member 5, pseudogene

Synonyms:

NBPF5; DKFZp434D177-like

SwissProt:

Q86XG9

WB Predicted band size:

41 kDa

WB Positive control:

Jurkat cells lysate

WB Recommended dilution:

500-3000