EFEMP2 Monoclonal Antibody (M37), Clone 1C2

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EFEMP2 Monoclonal Antibody (M37), Clone 1C2 EFEMP2 monoclonal antibody (M37), clone 1C2 Catalog # : H00030008-M37 規格 : [ 100 ug ] List All Specification Application Image Product Mouse monoclonal antibody raised against a full-length recombinant Western Blot (Recombinant protein) Description: EFEMP2. ELISA Immunogen: EFEMP2 (AAH10456.1, 26 a.a. ~ 443 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. Sequence: SPQDSEEPDSYTECTDGYEWDPDSQHCRDVNECLTIPEACKGEMKCIN HYGGYLCLPRSAAVINDLHGEGPPPPVPPAQHPNPCPPGYEPDDQDSCV DVDECAQALHDCRPSQDCHNLPGSYQCTCPDGYRKIGPECVDIDECRY RYCQHRCVNLPGSFRCQCEPGFQLGPNNRSCVDVNECDMGAPCEQRC FNSYGTFLCRCHQGYELHRDGFSCSDIDECSYSSYLCQYRCVNEPGRF SCHCPQGYQLLATRLCQDIDECESGAHQCSEAQTCVNFHGGYRCVDTN RCVEPYIQVSENRCLCPASNPLCREQPSSIVHRYMTITSERSVPADVFQIQ ATSVYPGAYNAFQIRAGNSQGDFYIRQINNVSAMLVLARPVTGPREYVLD LEMVTMNSLMSYRASSVLRLTVFVGAYTF Host: Mouse Reactivity: Human Isotype: IgG2a Kappa Quality Control Antibody Reactive Against Recombinant Protein. Testing: Western Blot detection against Immunogen (71.61 KDa) . Storage Buffer: In 1x PBS, pH 7.4 Storage Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. Instruction: Datasheet: Download Applications Western Blot (Recombinant protein) Protocol Download ELISA Gene Information Page 1 of 2 2016/5/23 Entrez GeneID: 30008 GeneBank BC010456.1 Accession#: Protein AAH10456.1 Accession#: Gene Name: EFEMP2 Gene Alias: FBLN4,MBP1,UPH1 Gene EGF-containing fibulin-like extracellular matrix protein 2 Description: Omim ID: 219100, 604633 Gene Ontology: Hyperlink Gene Summary: A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. [provided by RefSeq Other fibulin 4,fibulin-like extracellular matrix protein,mutant p53 binding Designations: protein 1 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 2016/5/23.
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