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Full name | CLDN19 rabbit polyclonal antibody |
Alternative names | 50 μl/100 μl |
Reactivity | rabbit polyclonal |
Applications | WB, IHC |
Host | Rabbit |
Clone type | rabbit polyclonal |
Target Background | 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. |
Swissprot No | Q8N6F1 |
Gene Accession | NP_683763 |
WB Predicted band size | |
WB Positive control | P109617-WB-1-P |
WB Recommended dilution | 23 kDa |
IHC predicted cell location | Predicted cell location: Cell membrane |
IHC positive control | Positive control: Human liver cancer |
IHC Recommed dilution | Recommended dilution: 10-50 |
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
P109617-WB-1-P
Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue or CLDN19 antigen-treated (Neutralization experiment) using P109617(CLDN19 Antibody) at dilution 1/30
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