RCAN1 antibody

Product Graph
Contáctenos para saber el precio

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

935106861
info@markelab.com
name
RCAN1 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab07201
tested applications
ELISA, WB, IHC

Description

Inhibits calcineurin-dependent transcriptional responses by binding to the catalytic domain of calcineurin A. Could play a role during central nervous system development.

Documents del producto

Instrucciones
Descargar
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
regulator of calcineurin 1 (RCAN1)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1:500-1:2000; IHC: 1:20-1:200
Clonality
polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
25-29 kDa
Purity
≥95% as determined by SDS-PAGE
Purification
Immunogen affinity purified
Size 1
100µg
Form
liquid
Tested Applications
ELISA, WB, IHC
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
UniProt ID
P53805
Gene ID
1827
Alias
Calcipressin-1,Adapt78,Down syndrome critical region protein 1,Myocyte-enriched calcineurin-interacting protein 1 (MCIP1),Regulator of calcineurin 1,RCAN1,ADAPT78,CSP1,DSC1,DSCR1
Background
Antibody anti-RCAN1
Status
RUO
Note
Mol. Weight 25-29 kDa

Descripción

Related Products

EH11742

Human RCAN1 (Calcipressin-1) ELISA Kit

Ver Producto
FNab07201

RCAN1 antibody

Inhibits calcineurin-dependent transcriptional responses by binding to the catalytic domain of calcineurin A. Could play a role during central nervous system development.

Ver Producto
abx004072

Calcipressin-1 (RCAN1) Antibody

RCAN1 Antibody is a Rabbit Polyclonal antibody against RCAN1. The protein encoded by this gene interacts with calcineurin A and inhibits calcineurin-dependent signaling pathways, possibly affecting central nervous system development. This gene is located in the minimal candidate region for the Down syndrome phenotype, and is overexpressed in the brain of Down syndrome fetuses. Chronic overexpression of this gene may lead to neurofibrillary tangles such as those associated with Alzheimer disease. Alternative splicing results in multiple transcript variants.

Ver Producto