TACSTD2 (Human) Recombinant Protein (P01)

TACSTD2 (Human) Recombinant Protein (P01)

TACSTD2 (Human) Recombinant Protein (P01) Catalog # : H00004070-P01 規格 : [ 10 ug ] [ 25 ug ] List All Specification Application Image Product Human TACSTD2 full-length ORF ( AAH09409, 27 a.a. - 323 a.a.) Enzyme-linked Immunoabsorbent Assay Description: recombinant protein with GST-tag at N-terminal. Western Blot (Recombinant Sequence: HTAAQDNCTCPTNKMTVCSPDGPGGRCQCRALGSGMAVDCSTLTSKC protein) LLLKARMSAPKNARTLVRPSEHALVDNDGLYDPDCDPEGRFKARQCNQ TSVCWCVNSVGVRRTDKGDLSLRCDELVRTHHILIDLRHRPTAGAFNHS Antibody Production DLDAELRRLFRERYRLHPKFVAAVHYEQPTIQIELRQNTSQKAAGDVDIG DAAYYFERDIKGESLFQGRGGLDLRVRGEPLQVERTLIYYLDEIPPKFSM Protein Array KRLTAGLIAVIVVVVVALVAGMAVLVITNRRKSGKYKKVEIKELGELRKEPS L Host: Wheat Germ (in vitro) Theoretical MW 58.41 (kDa): Preparation in vitro wheat germ expression system Method: Purification: Glutathione Sepharose 4 Fast Flow Quality Control 12.5% SDS-PAGE Stained with Coomassie Blue. Testing: Storage Buffer: 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. Storage Store at -80°C. Aliquot to avoid repeated freezing and thawing. Instruction: Note: Best use within three months from the date of receipt of this protein. MSDS: Download Datasheet: Download Applications Enzyme-linked Immunoabsorbent Assay Western Blot (Recombinant protein) Page 1 of 2 2016/5/21 Antibody Production Protein Array Gene Information Entrez GeneID: 4070 GeneBank BC009409 Accession#: Protein AAH09409 Accession#: Gene Name: TACSTD2 Gene Alias: EGP-1,GA733,GA733-1,M1S1,TROP2 Gene tumor-associated calcium signal transducer 2 Description: Omim ID: 137290, 204870 Gene Ontology: Hyperlink Gene Summary: This intronless gene encodes a carcinoma-associated antigen defined by the monoclonal antibody GA733. This antigen is a member of a family including at least two type I membrane proteins. It transduces an intracellular calcium signal and acts as a cell surface receptor. Mutations of this gene result in gelatinous drop-like corneal dystrophy, an autosomal recessive disorder characterized by severe corneal amyloidosis leading to blindness. [provided by RefSeq Other OTTHUMP00000011755,epithelial glycoprotein-1,membrane Designations: component, chromosome 1, surface marker 1 (40kD glycoprotein, identified by monoclonal antibody GA733) 服務條款 | 隱私權政策 | 著作及商標 | 網站地圖 ©2016 亞諾法生技股份有限公司 Abnova Corporation. 版權所有. Page 2 of 2 2016/5/21.

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