XPC ELISA Kit
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- Target See all XPC ELISA Kits
- XPC (Xeroderma Pigmentosum, Complementation Group C (XPC))
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Reactivity
- Human
- Detection Method
- Colorimetric
- Method Type
- Sandwich ELISA
- Detection Range
- 0.312 ng/mL - 20 ng/mL
- Minimum Detection Limit
- 0.312 ng/mL
- Application
- ELISA
- Sample Type
- Cell Lysate, Tissue Homogenate
- Analytical Method
- Quantitative
- Specificity
- This assay has high sensitivity and excellent specificity for detection of Xeroderma Pigmentosum, Complementation Group C (XPC). No significant cross-reactivity or interference between Xeroderma Pigmentosum, Complementation Group C (XPC) and analogues was observed.
- Sensitivity
- 0.114 ng/mL
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- Comment
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The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
- Assay Time
- 3 h
- Plate
- Pre-coated
- Protocol
- The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Xeroderma Pigmentosum, Complementation Group C (XPC). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Xeroderma Pigmentosum, Complementation Group C (XPC). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Xeroderma Pigmentosum, Complementation Group C (XPC), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Xeroderma Pigmentosum, Complementation Group C (XPC) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
- Assay Precision
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Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Xeroderma Pigmentosum, Complementation Group C (XPC) were tested 20 times on one plate, respectively
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Xeroderma Pigmentosum, Complementation Group C (XPC) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12% - Restrictions
- For Research Use only
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- Handling Advice
- The Stop Solution is acidic. Do not allow to contact skin or eyes. Calibrators, controls and specimen samples should be assayed in duplicate. Once the procedure has been started, all steps should be completed without interruption.
- Storage
- 4 °C,-20 °C
- Storage Comment
- -20°C. Bring all reagents to room temperature before beginning test. The kit may be stored at 4°C for immediate use within two days upon arrival. Reseal any unused strips with desiccant pack. Minimize freeze/thaw cycles.
- Expiry Date
- 4-8 months
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- Target See all XPC ELISA Kits
- XPC (Xeroderma Pigmentosum, Complementation Group C (XPC))
- Alternative Name
- Xeroderma Pigmentosum, Complementation Group C (XPC Products)
- Synonyms
- RAD4 ELISA Kit, XP3 ELISA Kit, XPCC ELISA Kit, XPC complex subunit, DNA damage recognition and repair factor ELISA Kit, xeroderma pigmentosum, complementation group C ELISA Kit, XPC ELISA Kit, Xpc ELISA Kit
- Background
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Gene Name: Xeroderma Pigmentosum, Complementation Group C
Gene Aliases: XP-C, XP3, XPCC, RAD4, Xeroderma Pigmentosum Group C Protein, DNA repair protein complementing XP-C cells
- Pathways
- p53 Signaling, DNA Damage Repair
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