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

Product Graph
195€ (100 µg)

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

935106861
info@markelab.com
name
B-Cell Receptor-Associated Protein 31 (BCAP31) Peptide
category
Proteins and Peptides
provider
Abbexa
reference
abx269144
tested applications
P-ELISA

Description

B-Cell Receptor-Associated Protein 31 (BCAP31) Peptide is a synthetic peptide. This peptide is used in the production of

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Immunogen Target
B-Cell Receptor-Associated Protein 31 (BCAP31)
Host
Synthetic
Assay Type
Activity: Not tested.
Sequence Fragment: C-Terminus: C-QAAVDGPMDKKEE
Recommended Dilution
BL (predicted): 0.5 mg/ml. Optimal dilutions/concentrations should be determined by the end user.
Conjugation
Unconjugated
Size 1
100 µg
Form
Lyophilized
Tested Applications
P-ELISA
Buffer
Prior to lyophilization: Deionized water.
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_001132929.1, NP_005736.3
OMIM
300398
Background
Protein 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.
Reconstitute in deionized water.

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