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028750 Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) BioAssay™ ELISA Kit (Human, Mouse, Rat)

Specifications
Brand
BioAssay™
Kit Type
Sandwich ELISA
Tests
96
Sample Volume
100ul
Sensitivity
26pg/ml
Detection Method
Colorimetric
Detection Range
78-5000pg/ml
Sample Matrix
Tissue homogenates and other biological fluids
EU Commodity Code
38220000
UN DOT Shipping
UN2796 PGII
Shipping Temp
Blue Ice
Storage Temp
4°C/-20°C

Intended Use
Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) BioAssay™ ELISA Kit (Rat) is a sandwich enzyme immunoassay for in vitro quantitative measurement of UCHL1 in rat tissue homogenates, cell lysates, cell culture supernates and other biological fluids. Due to the 96% homology of the sequence among different species, the kit is expected to crossreact with human and mouse samples.
Detection Range
0.78-50ng/ml
Sensitivity
0.28ng/ml
Intra-Assay CV
<10%
Inter-Assay CV
<12%
Kit Components
*028750A: Microtiter Strips, 1x96 wells *028750B: Standard, 2x1 vial 028750C: Standard Diluent, 1x20ml *028750D: Detection Reagent A (green), 1x120ul *028750E: Detection Reagent B (red), 1x120ul 028750F: Assay Diluent A, 1x12ml 028750G: Assay Diluent B, 1x12ml 028750H: TMB Substrate, 1x9ml 028750K: Stop Solution, 1x6ml 028750L: Wash Buffer, 30X, 1x20ml
Precaution
The Stop Solution (028750K) included for use in this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
Storage and Stability
Store *028750A, *028750B, *028750D and *028750E at -20°C. Store all the other components at 4°C. Unused kit is stable for 6 months after receipt. Once kit components are opened, it is highly recommended to use remaining reagents within 1 month provided this is within the expiration date of the kit. For maximum recovery of product, centrifuge the original vials after thawing and prior to removing the cap.
Assay Procedure Summary
1. Prepare all reagents, samples and standards. 2. Add 100ul standard or sample to each well. Incubate 2 hours at 37°C. 3. Aspirate and add 100ul prepared Detection Reagent A. Incubate 1 hour at 37°C. 4. Aspirate and wash 3 times. 5. Add 100ul prepared Detection Reagent B. Incubate 30 minutes at 37°C. 6. Aspirate and wash 5 times. 7. Add 90ul Substrate Solution. Incubate 15-25 minutes at 37°C. 8. Add 50ul Stop Solution. Read at 450nm immediately.
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