PRKDC ELISA Kit (Protein Kinase, DNA-Activated, Catalytic Polypeptide)

Details for Product PRKDC ELISA Kit No. ABIN5674824
Kits with alternative reactivity to:
Detection Method
Method Type
Sandwich ELISA
Detection Range
0.312 ng/mL - 20 ng/mL
Minimum Detection Limit
0.312 ng/mL
Sample Type Tissue Homogenate
Analytical Method Quantitative
Detection Method Colorimetric
Sensitivity 0125 ng/mL
Components Pre-coated, ready to use 96-well strip plate
Standard (freeze dried)
Standard Diluent
Detection Reagent A
Detection Reagent B
Assay Diluent A
Assay Diluent B
TMB Substhumane
Stop Solution
Wash Buffer(30 x concenthumane)
Plate sealer for 96 wells
Instruction manual
Material not included 1. Microplate reader with 450 ± 10nm filter.
2. Precision single or multi-channel pipettes and disposable tips.
3. Eppendorf Tubes for diluting samples.
4. Deionized or distilled water.
5. Absorbent paper for blotting the microtiter plate.
6. Container for Wash Solution.
Alternative Name Protein Kinase, DNA Activated, Catalytic Polypeptide (PRKDC) (PRKDC ELISA Kit Abstract)
Background Alternative name: HYRC, HYRC1, DNPK1, p350, DNAPK, XRCC7, DNA-PKcs
Gene ID 5591
UniProt P78527
Pathways DNA Damage Repair, Production of Molecular Mediator of Immune Response
Application Notes Optimal working dilution should be determined by the investigator.
Assay Time 1 - 4.5 h
Plate Pre-coated
Protocol 1. Prepare all reagents, samples and standards
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37℃
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37℃
4. Aspirate and wash 3 times
5. Add 100µL prepared Detection Reagent B. Incubate 1 hour at 37℃
6. Aspirate and wash 5 times
7. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37℃
8. Add 50µL Stop Solution. Read at 450nm immediately.
Restrictions For Research Use only
Storage 4 °C
Expiry Date 12 months