NBPF5 antibody (AA 302-351)

Catalog No. ABIN1535095

The Rabbit Polyclonal anti-NBPF5 antibody is suitable to detect NBPF5 in samples from Human, Rat and Mouse. It has been validated for WB, ELISA, IHC and IF.

Quick Overview for NBPF5 antibody (AA 302-351) (ABIN1535095)

Target: NBPF5 (Neuroblastoma Breakpoint Family, Member 5 (NBPF5))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NBPF5 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-NBPF5 Antibody

Binding Specificity: AA 302-351

Purpose: NBPF5 Antibody

Specificity: NBPF5 Polyclonal Antibody detects endogenous levels of NBPF5 protein.

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

Purity: > 95 %

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

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for NBPF5

Target: NBPF5 (Neuroblastoma Breakpoint Family, Member 5 (NBPF5))

Alternative Name: NBPF5

Background:

Synonyms: NBPF5, Neuroblastoma breakpoint family member 5

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. 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.

Gene Name: NBPF5

Protein Name: Neuroblastoma breakpoint family member 5

Molecular Weight: 40 kDa

Gene ID: 284610

UniProt: Q86XG9