NBPF6 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES9902
Catalog Number: ELK-ES9902
Reactivity: Human
Applications: WB, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Reactivity: Human
Applications: WB, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
neuroblastoma breakpoint family member 6(NBPF6) Homo sapiens 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. Gene copy number variations in the 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 fam
Immunogen: Synthesized peptide derived from human protein . at AA range: 360-440
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 70
GeneID: NBPF6
Storage: -20°C/1 year
NOTE: For Research Use Only
neuroblastoma breakpoint family member 6(NBPF6) Homo sapiens 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. Gene copy number variations in the 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 fam
Immunogen: Synthesized peptide derived from human protein . at AA range: 360-440
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 70
GeneID: NBPF6
Storage: -20°C/1 year
NOTE: For Research Use Only
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