NBPF3 antibody (N-Term)

Catalog No. ABIN5517639

Product Details anti-NBPF3 Antibody

Target: NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))

Binding Specificity: N-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NBPF3 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: CDQVKKEDQE ATSPRLSREL LDEKEPEVLQ DSLDRFYSTP FEYLELPDLC

Predicted Reactivity: Human: 100%

Characteristics: This is a rabbit polyclonal antibody against NBPF3. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human NBPF3

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for NBPF3

Target: NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))

Alternative Name: NBPF3 (NBPF3 Products)

Synonyms: AE2 antibody, NBPF member 3 antibody, NBPF3 antibody

Background: 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. DUF1220 copy number variations in 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 family contains numerous pseudogenes.

Alias Symbols: NBPF3, L7,

Protein Interaction Partner: NBPF3, APP, UBD, UBC, TSEN15, ANK1, EWSR1,

Protein Size: 275

Gene ID: 84224