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Invitrogen™ Claudin 19 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5101526
Description
Antibody detects endogenous levels of total CLDN19.
The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010].
Specifications
Claudin 19 | |
Polyclonal | |
Unconjugated | |
CLDN19 | |
claudin 19; claudin-19; Cldn19; HOMG5 | |
Rabbit | |
Affinity Chromatography | |
RUO | |
149461, 298487 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
Q5QT56, Q8N6F1 | |
CLDN19 | |
A synthesized peptide derived from human CLDN19(Accession Q8N6F1), corresponding to amino acid residues V85-T135. | |
100 μL | |
Primary | |
Human, Rat | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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