catalog number :
MBS426683
products full name :
Actin-like 7B Immunizing Peptide
products short name :
Actin-like 7B
products name syn :
actin-like 7B; ACTL7B; RP11-3J11.2; actin-like 7-beta; Actin-like 7B; Actin-like 7B
other names :
actin-like protein 7B; Actin-like protein 7B; actin-like protein 7B; actin like 7B; Actin-like-7-beta
products gene name :
ACTL7B
other gene names :
ACTL7B; ACTL7B; Tact1
uniprot entry name :
ACL7B_HUMAN
sequence :
C-QLKMKPRKVHKIK
form :
100ug of dried peptide
storage stability :
Shipped at ambient temperature, store at -20 degree C
ncbi acc num :
NP_006677.1
ncbi gb acc num :
NM_006686.3
ncbi mol weight :
45,234 Da
ncbi summary :
The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known. [provided by RefSeq, Jul 2008]
uniprot summary :
ACTL7B: is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known. [provided by RefSeq, Jul 2008]. Protein type: Motility/polarity/chemotaxis; Cytoskeletal. Chromosomal Location of Human Ortholog: 9q31. Cellular Component: actin cytoskeleton; cytoplasm. Molecular Function: structural constituent of cytoskeleton