ARG67369

anti-Claudin 4 antibody [SQab30404]

anti-Claudin 4 antibody [SQab30404] for IHC-Formalin-fixed paraffin-embedded sections and Human

Overview

Product Description Rabbit Monoclonal antibody [SQab30404] recognizes Claudin 4
Tested Reactivity Hu
Tested Application IHC-P
Host Rabbit
Clonality Monoclonal
Clone SQab30404
Isotype IgG
Target Name Claudin 4
Antigen Species Human
Immunogen Synthetic peptide
Conjugation Un-conjugated
Alternate Names CPE-R; Williams-Beuren syndrome chromosomal region 8 protein; hCPE-R; CPE-receptor; CPETR; CPETR1; Clostridium perfringens enterotoxin receptor; Claudin-4; CPER; WBSCR8

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:100 - 1:200
Application Note IHC-P: Antigen Retrieval: Heat mediation was performed in Tris/EDTA buffer (pH 9.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity chromatography purified
Buffer PBS, 0.01% Sodium azide, 40% Glycerol and 0.05% BSA.
Preservative 0.01% Sodium azide
Stabilizer 40% Glycerol and 0.05% BSA
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 1364 Human CLDN4

Swiss-port # O14493 Human Claudin-4

Gene Symbol CLDN4
Gene Full Name claudin 4
Background The protein encoded by this intronless gene belongs to the claudin family. Claudins are integral membrane proteins that are components of the epithelial cell tight junctions, which regulate movement of solutes and ions through the paracellular space. This protein is a high-affinity receptor for Clostridium perfringens enterotoxin (CPE) and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems. [provided by RefSeq, Sep 2013]
Function Plays a major role in tight junction-specific obliteration of the intercellular space. [UniProt]
Cellular Localization Cell junction, tight junction, Cell membrane, Multi-pass membrane protein. [UniProt]
Calculated MW 22 kDa
PTM Phosphorylated. Phosphorylation by EPHA2 is stimulated by EFNA1 and alters interaction with TJP1. [UniProt]