B-Cell Receptor-Associated Protein 31 (BCAP31) Antibody

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292.5€ (80 µl)

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935106861
info@markelab.com
name
B-Cell Receptor-Associated Protein 31 (BCAP31) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx034875
tested applications
ELISA, WB, IHC

Description

May play a role in anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi. May be involved in CASP8-mediated apoptosis.

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: KLH-conjugated synthetic peptide between 120-147 amino acids from the Central region of human BCAP31.
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/1000, IHC-P: 1/25. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
Calculated MW: 28 kDa
Purification
Purified through a protein A column, followed by peptide affinity purification.
Size 1
80 µl
Size 2
400 µl
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS containing 0.09% sodium azide.
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
NCBI Accession
NP_001132913.1, NP_001132929.1, NP_001243376.1, NP_005736.3
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

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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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