α-HydroxybutyrateDehydrogenaseAssayKitisanAssayKitbyLatexEnhancedMethod.Basedonthebottletype,productmodelcanbeclassifiedintoHitachi7170,Hitachi7060,Hitachi7020,Beckman,Toshiba,Mindray,DuPont,Innova,Siemens,KHB,Abbott,Universaltypes,etc.Thisreagentisusedtodeterminetheα-HydroxybutyrateDehydrogenaseactivityinhumanserum.Underthecatalysisofα-HydroxybutyrateDehydrogenase,α-Ketobutyricacidisreducedtoα-hydroxybutyricacid,andNADHisoxidizedtoNAD+.At340nm,thedecreaserateofabsorbanceisdirectlyproportionaltoα-hydroxybutyratedehydrogenaseactivity,andtheα-hydroxybutyratedehydrogenaseactivityinthesamplecanbecalculatedbymonitoringtheabsorbancedecreasingrate.

R1:DetectionReagent1	R2:DetectionReagent2
TrisBuffer󑴔.1g/l	NADH→Appropriate
α-ketobutyricacid→0.306g/L

26S Proteasome Complex Subunit SEM1 (SEM1) shRNA abx972681  Specificity: SHFM1 shRNA Plasmid (Mouse) contains 3 different target-specific plasmids each encoding 19-23 nt (plus hairpin) shRNAs designed to knock down gene expression. Each plasmid contains a resistance gene for the selection of cells stably expressing shRNA. Form: Lyophilized