CLDN19 Monoclonal Antibody (M02), Clone 2F2

CLDN19 Monoclonal Antibody (M02), Clone 2F2

CLDN19 monoclonal antibody (M02), clone 2F2 Catalog # : H00149461-M02 規格 : [ 100 ug ] List All Specification Application Image Product Mouse monoclonal antibody raised against a full-length recombinant Western Blot (Recombinant protein) Description: CLDN19. Sandwich ELISA (Recombinant Immunogen: CLDN19 (AAH30524, 1 a.a. ~ 211 a.a) full-length recombinant protein protein) with GST tag. MW of the GST tag alone is 26 KDa. Sequence: MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGL WMSCASQSTGQVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLS VVGMKCTRVGDSNPIAKGRVAIAGGALFILAGLCTLTAVSWYATLVTQEF FNPSTPVNARYEFGPALFVGWASAGLAVLGGSFLCCTCPEPERPNSSP QPYRPGPSAAAREYV enlarge Host: Mouse ELISA Reactivity: Human Isotype: IgG2a Kappa Quality Control Antibody Reactive Against Recombinant Protein. Testing: Western Blot detection against Immunogen (48.95 KDa) . Storage Buffer: In 1x PBS, pH 7.4 Storage Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. Instruction: MSDS: Download Datasheet: Download Applications Western Blot (Recombinant protein) Protocol Download Sandwich ELISA (Recombinant protein) Page 1 of 2 2018/11/27 Detection limit for recombinant GST tagged CLDN19 is 0.1 ng/ml as a capture antibody. Protocol Download ELISA Gene Information Entrez GeneID: 149461 GeneBank BC030524 Accession#: Protein AAH30524 Accession#: Gene Name: CLDN19 Gene Alias: - Gene claudin 19 Description: Omim ID: 248190, 610036 Gene Ontology: Hyperlink Gene Summary: 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 Other OTTHUMP00000008733 Designations: Gene Pathway Cell adhesion molecules (CAMs) Leukocyte transendothelial migration Tight junction 服務條款 | 隱私權政策 | 著作及商標 | 網站地圖 ©2018 亞諾法生技股份有限公司 Abnova Corporation. 版權所有. Page 2 of 2 2018/11/27.

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