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Claudin 19 Rabbit anti-Human, Polyclonal, Bioss
SDP

Rabbit Polyclonal Antibody

Supplier:  Bioss BS13749R

Encompass_Preferred

Catalog No. 50-198-3130


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Description

Description

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

Specifications

Claudin 19
Polyclonal
Unconjugated
CLDN19
BOS_3650; claudin 19; Claudin-19; CLDN19; HOMG5; LOC100357396
Rabbit
Protein A
RUO
149461
-20°C
Liquid
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
1 μg/mL
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Q8N6F1
CLDN19
KLH conjugated synthetic peptide derived from human Claudin 19.
100 μL
Primary
Human
Antibody
IgG
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