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Validated All-in-One™ qPCR Primer for APOBEC3B(NM_004900.4) Search again
Product ID:
HQP022939
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
A3B, APOBEC1L, ARCD3, ARP4, DJ742C19.2, PHRBNL, bK150C2.2
Gene Description:
apolipoprotein B mRNA editing enzyme catalytic subunit 3B
Target Gene Accession:
NM_004900.4(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Summary
This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22.
Gene References into function
- different APOBEC3 family members function to neutralize specific lentiviruses
- APOBEC3B reduces retrotransposition by the intracisternal A-particle.
- APOBEC3B and APOBEC3F have roles in inhibiting L1 retrotransposition by a DNA deamination-independent mechanism
- separation of function of the cytidine deaminase domains is maintained in hA3B and hA3F, but roles of the two domains are reversed in mouse A3
- detailed sequence and population genetic analysis of a 29.5-kb common human deletion polymorphism that removes the APOBEC3B gene.
- HIV-1 Vif(IIIB) induces the emigration from the nucleus to the cytosol and thereby causes net increases in the cytosolic concentrations and anti-HIV-1 activities of APOBEC3A and APOBEC3B.
- only the carboxy-terminal deaminase domain of APOBEC3B catalyses cytidine deaminations leading to hepatitis B virus (HBV) hypermutations;induction of hypermutations is not sufficient for full inhibition of HBV replication; both domains of must be intact
- study provides evidence of editing of human papillomavirus 1a and 16 DNA by APOBEC3 in plantar warts and precancerous cervix biopsies
