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Claudin 3 Rabbit Polyclonal Antibody

CAT: 0013-GTR18108867-01Size: 30 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18108867-01Size:30 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
The Claudin 3 Antibody is suitable for IF, IHC, IP, WB. It is a Polyclonal, Unconjugated antibody which raised against KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human Claudin 3. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography.
Product Name Alternative
C7orf1; CPETR2; Claudin-3; Clostridium perfringens enterotoxin receptor 2; CPE-R 2; CPE-receptor 2; Rat ventral prostate.1 protein homolog; hRVP1
UniProt
O15551
Reactivity
Bovine, Human, Mouse, Rat
Immunogen
KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human Claudin 3. The exact sequence is proprietary.
Target
CLDN3
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Cardiovascular Disease, Epigenetics
Purification
The antibody was purified by immunogen affinity chromatography.
Dilution
WB: 1:500-1000, IHC-P: 1:100-200, IF/ICC: 1:100-500, IP: 1:10-100
Form
Liquid
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
IF, IHC, IP, WB
Host or Source
Rabbit
Preservative
0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Entrez
1365

UniProtKB · O15551

Claudin-3

CLD3_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O15551
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CLDN3
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
—
Protein keywords

Cellular component

Cell junctionCell membraneMembraneTight junction

PTM

Phosphoprotein

Technical term

Proteomics identificationReference proteome

Domain

TransmembraneTransmembrane helix

Disease

Williams-Beuren syndrome

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