Low Affinity Nerve Growth Factor Receptor (LNGFR) BioAssay(TM) ELISA Kit (Mouse)

Produktübersicht

• Artikelname: Low Affinity Nerve Growth Factor Receptor (LNGFR) BioAssay(TM) ELISA Kit (Mouse)
• Artikelnummer: USB-366277
• Hersteller Artikelnummer: 366277
• Alternativnummer: USB-366277-96
• Hersteller: US Biological
• Kategorie: Kits/Assays
• Applikation: ELISA

Produktbeschreibung

The Low Affinity Nerve Growth Factor Receptor (LNGFR) BioAssay(TM) ELISA Kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of mouse LNGFR in serum, plasma, tissue homogenates and other biological fluids. Detection Range: 0.156-10ng/ml Sensitivity: 0.058ng/ml Specificity: This assay has high sensitivity and excellent specificity for detection of Low Affinity Nerve Growth Factor Receptor (LNGFR). No significant cross-reactivity or interference between Low Affinity Nerve Growth Factor Receptor (LNGFR) and analogues was observed. Precision: Intra-Assay %CV: <10% Inter-Assay %CV: <12% Kit Components: Pre-coated, ready to use 96-well strip plate Standard, 2x vials Detection Reagent A, 1x120ul Detection Reagent B, 1x120ul TMB Substrate, 1x9ml Wash Buffer (30X): 1x20ml Standard Diluent, 1x20ml Assay Diluent A, 1x12ml Assay Diluent B, 1x12ml Stop Solution, 1x6ml Storage and Stability: Store Microtiter Strips, Standard, Detection Reagents and Positive Control at -20C. After reconstitution of Positive Control, store at 4C and use within 5 days. Store all the other components at 4C. 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 37C. 3. Aspirate and add 100ul prepared Detection Reagent A immediately. Incubate 1 hour at 37C. 4. Aspirate and wash 3 times. 4. Add 100ul prepared Detection Reagent B. Incubate 30 minutes at 37C. 5. Aspirate and wash 5 times. 6. Add 90ul Substrate Solution. Incubate 15-25 minutes at 37C. 7. Add 50ul Stop Solution. Read at 450nm immediately.