B-Cell Receptor-Associated Protein 34 (BAP31) Antibody

Product Graph
364€ (100 µg)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
B-Cell Receptor-Associated Protein 34 (BAP31) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx230802
tested applications
ELISA, WB, IHC, IF/ICC, FCM, IP

Description

BAP31 Antibody is a Rabbit Polyclonal against BAP31.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
B-Cell Receptor-Associated Protein 34 (BAP31)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/1000 - 1/6000, IHC: 1/50 - 1/500, IF/ICC: 1/50 - 1/500, IP: 1/500 - 1/3000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purity
≥ 95% (SDS-PAGE)
Purification
Purified by immunogen affinity chromatography.
Size 1
100 µg
Form
Liquid
Tested Applications
ELISA, WB, IHC, IF/ICC, FCM, IP
Buffer
PBS, pH 7.3, with 0.02% sodium azide and 50% glycerol.
Availability
Shipped within 5-12 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P51572
Alias
BCAP31, 6C6-AG, BAP31, CDM, DDCH
Background
Antibody anti-BCAP31
Status
RUO
Note
Concentration: 2 mg/ml - Validity: 12 months.

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