B-cell receptor-associated protein 31 (BCAP31) Antibody

299€ (50 µl)
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
935106861
info@markelab.com
name
B-cell receptor-associated protein 31 (BCAP31) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx402429
tested applications
ELISA, WB, IHC, IF/ICC, FCM
Description
B-cell receptor-associated protein 31 (BCAP31) Antibody is a Recombinant Rabbit Monoclonal antibody for the detection of Human BCAP31.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | B-cell receptor-associated protein 31 (BCAP31) |
Host | Rabbit |
Reactivity | Human |
Recommended Dilution | WB: 1/500 - 1/2000, IHC: 1/50 - 1/200, IF/ICC: 1/50 - 1/200, FCM: 1/50 - 1/200. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Monoclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Expression | Recombinant |
Purification | Purified by affinity chromatography. |
Size 1 | 50 µl |
Size 2 | 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB, IHC, IF/ICC, FCM |
Buffer | PBS, pH 7.4, 150 mM NaCl, 0.02% sodium azide and 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P51572 |
Background | Antibody anti-BCAP31 |
Status | RUO |
Descripción
Related Products

BCAP31 antibody
Ver Producto
Recombinant Human BCAP31
Ver Producto
B-Cell Receptor-Associated Protein 31 (BCAP31) Antibody
BCAP31 Antibody is a Rabbit Polyclonal antibody against BCAP31. 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.
Ver Producto