Anti-BCAP31 Antibody (CAB7056)
- SKU:
- CAB7056
- Product type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Death
Description
Antibody Name: | Anti-BCAP31 Antibody |
Antibody SKU: | CAB7056 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IF IP |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 127-246 of human BCAP31 (NP_001243376.1). |
Application: | WB IF IP |
Recommended Dilution: | WB 1:500 - 1:2000 IF 1:50 - 1:100 IP 1:50 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | MCF-7, HT-29, SH-SY5Y, HeLa, A-431, Mouse liver, Mouse kidney, Mouse lung, Rat brain |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 127-246 of human BCAP31 (NP_001243376.1). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | ATLL ASNE AFKK QAES ASEA AKKY MEEN DQLK KGAA VDGG KLDV GNAE VKLE EENR SLKA DLQK LKDE LAST KQKL EKAE NQVL AMRK QSEG LTKE YDRL LEEH AKLQ AAVD GPMD KKEE |
Gene ID: | 10134 |
Uniprot: | P51572 |
Cellular Location: | Endoplasmic reticulum membrane, Endoplasmic reticulum-Golgi intermediate compartment membrane, Multi-pass membrane protein |
Calculated MW: | 27kDa/34kDa |
Observed MW: | 28kDa |
Synonyms: | BCAP31, 6C6-AG, BAP31, CDM, DDCH, DXS1357E |
Background: | 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. |
UniProt Protein Function: | BCAP31 iso2: May play a role in anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi. May be involved in CASP8-mediated apoptosis. Homodimer and heterodimer with BCAP29. Binds CASP8 (isoform 9) as a complex containing BCAP31, BCAP29, BCL2 and/or BCL2L1. Interacts with VAMP3, VAMP1 and membrane IgD immunoglobulins. May interact with ACTG1 and non-muscle myosin II. Interacts with PTPLB. Ubiquitous. Belongs to the BCAP29/BCAP31 family. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Membrane protein, integral; Membrane protein, multi-pass Chromosomal Location of Human Ortholog: Xq28 Cellular Component: endoplasmic reticulum membrane; ER-Golgi intermediate compartment membrane; membrane; clathrin-coated vesicle; endoplasmic reticulum; integral to plasma membrane; lipid particle; cytosol Molecular Function:protein binding; MHC class I protein binding; protein complex binding Biological Process: intracellular protein transport; ER to Golgi vesicle-mediated transport; antigen processing and presentation of peptide antigen via MHC class I; elevation of cytosolic calcium ion concentration; apoptosis; reduction of endoplasmic reticulum calcium ion concentration; positive regulation of caspase activity; spermatogenesis; cell structure disassembly during apoptosis; elevation of mitochondrial calcium ion concentration Disease: Deafness, Dystonia, And Cerebral Hypomyelination |
NCBI Summary: | 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. [provided by RefSeq, Jan 2012] |
UniProt Code: | P51572 |
NCBI GenInfo Identifier: | 1705725 |
NCBI Gene ID: | 10134 |
NCBI Accession: | P51572.3 |
UniProt Secondary Accession: | P51572,Q13836, Q96CF0, B3KQ79, D3DWV5, |
UniProt Related Accession: | P51572 |
Molecular Weight: | 34,752 Da |
NCBI Full Name: | B-cell receptor-associated protein 31 |
NCBI Synonym Full Names: | B-cell receptor-associated protein 31 |
NCBI Official Symbol: | BCAP31 |
NCBI Official Synonym Symbols: | CDM; DDCH; BAP31; 6C6-AG; DXS1357E |
NCBI Protein Information: | B-cell receptor-associated protein 31; p28 Bap31; BCR-associated protein Bap31; 6C6-AG tumor-associated antigen |
UniProt Protein Name: | B-cell receptor-associated protein 31 |
UniProt Synonym Protein Names: | 6C6-AG tumor-associated antigen; Protein CDM; p28 |
Protein Family: | B-cell receptor-associated protein |
UniProt Gene Name: | BCAP31 |
UniProt Entry Name: | BAP31_HUMAN |