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

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299€ (50 µl)

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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
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Product specifications

Category
Primary Antibodies
Immunogen Target
Target: B-cell receptor-associated protein 31 (BCAP31)
Immunogen: A synthesized peptide derived from human 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
Gene ID
10134
OMIM
300398
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

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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.

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