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enabling C7 to insert into the pathogen's phospholipid bilayer
Add in each dilution tube 230uL Standard dilution ( 1× )
Source Rat Synonym Rat Calprotectin ELISA Kit Detection Type Double antibody sandwich method Composition Name 9 6 T match set remark Pre-coating 96 Well plate 8 Hole ×12 Strip without Standard 2 branch Dilute as per instructions
and HRP conjugate are sequentially added to microwells pre-coated with Beta-Site APP Cleaving Enzyme 2 (BACE2) capture antibody
Proto-oncogene c-ErbB-1
Human TFF2 ELISA Kit Size:96T enabling C7 to insert intoProduct Specification Usage Experimental equipment required for the experiment: 1. Microplate reader (450nm) 2. High precision pipette and gun tips: 0. 5 10uL, 5 50uL, 20 200uL, 200 1000uL 3. 37 constant temperature box 4. Distilled water or deionized water Sample processing and requirements: 1. Serum: Place the whole blood sample collected in the serum separation tube at room temperature for 2 hours or at 4 overnight, then centrifuge at 1000g for 20