CLDN4 polyclonal antibody
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More Files
- More Functions
Western Blot (Cell lysate)
Western blot analysis of CLDN4 polyclonal antibody (Cat # PAB27036) in extracts from HeLa cells.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical analysis of CLDN4 polyclonal antibody (Cat # PAB27036) in paraffin-embedded human breast carcinoma tissue.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of CLDN4.
Immunogen
A synthetic peptide corresponding to human CLDN4.
Host
Rabbit
Theoretical MW (kDa)
22
Reactivity
Human, Mouse, Rat
Specificity
CLDN4 polyclonal antibody detects endogenous levels of CLDN4 protein.
Form
Liquid
Purification
Antigen affinity purification
Concentration
1 mg/mL
Recommend Usage
Western Blot (1:500-1:1000)
Immunohistochemistry (1:50-1:200)
Immunofluorescence (1:50-1:200)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (0.05% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western blot analysis of CLDN4 polyclonal antibody (Cat # PAB27036) in extracts from HeLa cells.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical analysis of CLDN4 polyclonal antibody (Cat # PAB27036) in paraffin-embedded human breast carcinoma tissue.Enzyme-linked Immunoabsorbent Assay
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Gene Info — CLDN4
Entrez GeneID
1364Protein Accession#
O14493Gene Name
CLDN4
Gene Alias
CPE-R, CPER, CPETR, CPETR1, WBSCR8, hCPE-R
Gene Description
claudin 4
Omim ID
602909Gene Ontology
HyperlinkGene Summary
This gene encodes an integral membrane protein, which belongs to the claudin family. The protein is a component of tight junction strands 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
Other Designations
Clostridium perfringens enterotoxin receptor 1|Williams-Beuren syndrome chromosomal region 8 protein
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Interactome
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Pathway
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