Western Blot: Claudin-19 Antibody (2F2) [H00149461-M02] - Detection against Immunogen (48.95 KDa) .
Immunocytochemistry/ Immunofluorescence: Claudin-19 Antibody (2F2) [H00149461-M02] - Tight junction proteins and the transepithelial resistance of iPSC-RPE. RPE cells were cultured on laminin-coated Transwell inserts. ...read more
ELISA: Claudin-19 Antibody (2F2) [H00149461-M02] - Detection limit for recombinant GST tagged CLDN19 is 0.1 ng/ml as a capture antibody.
Immunocytochemistry/ Immunofluorescence: Claudin-19 Antibody (2F2) [H00149461-M02] - Tight junction proteins & the transepithelial resistance of iPSC-RPE. RPE cells were cultured on laminin-coated Transwell inserts. a ...read more
CLDN19 (AAH30524, 1 a.a. ~ 211 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTGQVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAIAGGALFILAGLCTLTAVSWYATLVTQEFFNPSTPVNARYEFGPALFVGWASAGLAVLGGSFLCCTCPEPERPNSSPQPYRPGPSAAAREYV
Specificity
CLDN19 - claudin 19 (2F2)
Isotype
IgG2a Kappa
Clonality
Monoclonal
Host
Mouse
Gene
CLDN19
Purity
IgG purified
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Antibody Reactive Against Recombinant Protein with GST tag on ELISA and Western Blot. GST tag alone is used as a negative control. Immunocytochemistry/Immunofluorescence was reported in scientific literature.
Publications
Read Publications using H00149461-M02 in the following applications:
Mouse reactivity reported in scientific literature (PMID: 28524846).
Packaging, Storage & Formulations
Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
In 1x PBS, pH 7.4
Preservative
No Preservative
Purity
IgG purified
Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for Claudin-19 Antibody (2F2)
claudin 19
Claudin19
Claudin-19
CLDN19
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. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq]
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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