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

Product Graph
260€ (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
abx213291
tested applications
ELISA, WB, IHC

Description

BCAP31 Antibody is a Rabbit Polyclonal against BCAP31.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Target: B-cell receptor-associated protein 31 (BCAP31)
Immunogen: Fusion protein of human BCAP31.
Host
Rabbit
Reactivity
Human, Mouse
Recommended Dilution
ELISA: 1/2000 - 1/5000, WB: 1/500 - 1/2000, IHC: 1/50 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
50 µl
Size 2
100 µl
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS, pH 7.4, containing 0.05% NaN3 and 40% 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
Gene ID
10134
OMIM
300398
Alias
BCAP31, 6C6-AG, BAP31, CDM, DDCH
Background
Antibody anti-BCAP31
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

Related Products

FNab00802

BCAP31 antibody

Ver Producto
P2494

Recombinant Human BCAP31

Ver Producto
abx005340

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