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BCAP31 encodes a member of the B-cell receptor associated protein 31 superfamily. Additionally we are shipping B-Cell Receptor-Associated Protein 31 Antibodies (131) and B-Cell Receptor-Associated Protein 31 Kits (3) and many more products for this protein.
Showing 9 out of 12 products:
Human BCAP31 Protein expressed in Escherichia coli (E. coli) - ABIN1046592
Shtivelman, Lifshitz, Gale, Roe, Canaani: Alternative splicing of RNAs transcribed from the human abl gene and from the bcr-abl fused gene. in Cell 1986
Show all 2 references for ABIN1046592
The C-terminal domain of BAP31 is exposed on the cell surface of mouse embryonic stem cells.
BAP31/CDIP1-mediated regulation of mitochondrial apoptosis pathway represents a mechanism for establishing an ER-mitochondrial crosstalk for ER-stress-mediated apoptosis.
Data suggest that endoplasmic reticulum-localized Bcl2 (show BCL2 Proteins) protects against a Bax (show BAX Proteins)/Bak (show BAK1 Proteins)-independent cell death pathway initiated by the p20 (show HSPB6 Proteins) fragment of Bap31.
A high-molecular-weight complex of membrane proteins BAP29/BAP31 is involved in the retention of membrane-bound IgD in the endoplasmic reticulum.
results are consistent with the view that class I molecules are largely recruited to ER exit sites by Bap29/31, and that Bap29/31 is a cargo receptor for MHC class I molecules
p20 (show HSPB6 Proteins) BAP31 can operate upstream of BCL-2 (show BCL2 Proteins) in living cells to influence cell surface properties due to its effects on protein egress from the endoplasmic reticulum
These results suggest that a compositional change of AMPA (show GRIA3 Proteins) receptor (increase of GluR1 (show GRIA1 Proteins)) and upregulation of the Bap31 gene may be implicated in fatigue in mice.
interaction of P450 (show POR Proteins) 2C2 with BAP31 is important for its ER retention and expression level and that BAP31 may be involved in the regulation of apoptosis induced by the ER overload response to increased expression of P450 (show POR Proteins).
The C-terminal domain of BAP31 is exposed on the cell surface of human embryonic stem cells.
both BCAP31 and ABCD1 were associated with hepatic cholestasis and death before 1 year. Remarkably, a patient with an isolated deletion at the 3'-end of SLC6A8 (show SLC6A8 Proteins) had a similar severe phenotype as seen in BCAP31 deficiency
Transfected human respiratory syncytial virus SH protein co-localizes with transfected BAP31 in cells, and pulls down endogenous BAP31.
These findings provide, for the first time, mechanistic insights into how BAP31 regulates human embryonic stem cell stemness and survival via control of EpCAM (show EPCAM Proteins) expression.
Hypomethylation in BCAP31 is associated with breast cancer.
the lack of BAP31 disturbs endoplasmic reticulum (ER) metabolism and impacts the Golgi apparatus, highlighting an important role for BAP31 in ER-to-Golgi crosstalk.
BAP31 and BiP (show GDF10 Proteins) are essential for dislocation of SV40 from the endoplasmic reticulum to the cytosol.
Membrane-Associated RING-CH proteins MARCH VIII (show MARCH8 Proteins) and MARCH IV (show MARCH4 Proteins) associate with Bap31 and target CD81 (show CD81 Proteins) and CD44 (show CD44 Proteins) to lysosomes
Fis1 (show FIS1 Proteins) and Bap31 bridge the mitochondria-ER interface to establish a platform for apoptosis induction.
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
The data provide the first functional assessment of the role of caldesmon (show CALD1 Proteins) in cardiac development in vivo, and indicate that caldesmon (show CALD1 Proteins) is essential for proper cardiac organogenesis and function.
This gene encodes a member of the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein of the endoplasmic reticulum that is involved in the anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16.
, lipopeptide mating pheromone precursor bap3-1
, B-cell receptor-associated protein 31
, BCR-associated protein 31
, accessory protein BAP31
, 6C6-AG tumor-associated antigen
, BCR-associated protein Bap31
, p28 Bap31