NBPF3 anticorps (N-Term)

N° du produit ABIN5517639

Cet anticorps Lapin Polyclonal détecte spécifiquement NBPF3 dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour NBPF3 anticorps (N-Term) (ABIN5517639)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NBPF3 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-NBPF3 anticorps

Épitope: N-Term

Séquence: CDQVKKEDQE ATSPRLSREL LDEKEPEVLQ DSLDRFYSTP FEYLELPDLC

Homologie: Human: 100%

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur NBPF3

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

Autre désignation: NBPF3

Sujet: 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

ID gène: 84224