Trafficking Protein Particle Complex Subunit 2 (TRAPPC2) Antibody

Product Graph
364€ (100 µg)

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

935106861
info@markelab.com
name
Trafficking Protein Particle Complex Subunit 2 (TRAPPC2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx238945
tested applications
ELISA, WB, IP

Description

TRAPPC2 Antibody is a Rabbit Polyclonal against TRAPPC2.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Trafficking Protein Particle Complex Subunit 2 (TRAPPC2)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/500 - 1/5000, IP: 1/200 - 1/2000. 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, 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
P0DI81
Gene ID
6399
OMIM
300202
Background
Antibody anti-TRAPPC2
Status
RUO
Note
Concentration: 2 mg/ml - Validity: 12 months.

Descripción

Related Products

FNab08945

TRAPPC2 antibody

TRAPPC2 is one component of the TRAPP multisubunit tethering complex involved in intracellular vesicle trafficking [PMID:21525244]. It acts as an adaptor for the TRAPP complex in mammalian cells, mediating interactions with both TRAPPC9 and TRAPPC8. It prevents transcriptional repression and induction of cell death by ENO1. Also it plays a role in vesicular transport from endoplasmic reticulum to Golgi.

Ver Producto
P4653

Recombinant Human TRAPPC2

Ver Producto
abx025035

Trafficking Protein Particle Complex Subunit 2 (TRAPPC2) Antibody

TRAPPC2 is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y.

Ver Producto