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Home / ELISA Kit

Human DNA repair protein complementing XP-C cells (XPC) ELISA Kit

SKU : BHE13702233

Xeroderma pigmentosum, complementation group C, also known as XPC, is a component of the nucleotide excision repair (NER) pathway. There are multiple components involved in the NER pathway, including Xeroderma pigmentosum (XP) A-G and V, Cockayne syndrome (CS) A and B, and trichothiodystrophy (TTD) group A, etc.
This component, XPC, plays an important role in the early steps of global genome NER, especially in damage recognition, open complex formation, and repair protein complex formation.Mutations in this gene or some other NER components result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age.

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Mfr.No.	KTE60013
Description	This Human DNA repair protein complementing XP-C cells (XPC) ELISA Kit employs a two-site sandwich ELISA to quantitate XPC.
Alternative Names	XPC; RAD4; XP3; XPCC; xeroderma pigmentosum group C protein
Reactivity	Human
Detection Method	Colorimetric
Sample Type	Other biological fluids, Cell culture supernatants, Serum, Plasma
Assay Type	Sandwich (quantitative)
Assay Duration	Multiple steps standard sandwich ELISA assay with a working time of 3-5 hours. It depends on the experience of the operation person.
Kit Components	Human DNA repair protein complementing XP-C cells microplate Human DNA repair protein complementing XP-C cells standard Human DNA repair protein complementing XP-C cells detect antibody Streptavidin-HRP Standard diluent Assay buffer HRP substrate Stop solution Wash buffer Plate covers
Features	Human DNA repair protein complementing XP-C cells (XPC) ELISA Kit has high sensitivity and excellent specificity for detection of Human XPC. No significant cross-reactivity or interference between Human XPC and analogues was observed.
Calibration Range	Please inquire
Limit Of Detection	Please inquire
Precautions	The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.
Background	Xeroderma pigmentosum, complementation group C, also known as XPC, is a component of the nucleotide excision repair (NER) pathway. There are multiple components involved in the NER pathway, including Xeroderma pigmentosum (XP) A-G and V, Cockayne syndrome (CS) A and B, and trichothiodystrophy (TTD) group A, etc. This component, XPC, plays an important role in the early steps of global genome NER, especially in damage recognition, open complex formation, and repair protein complex formation.Mutations in this gene or some other NER components result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age.
Notes	This Human DNA repair protein complementing XP-C cells (XPC) ELISA Kit employs a two-site sandwich ELISA to quantitate XPC in samples. An antibody specific for XPC has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyXPC present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for XPC is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of XPC bound in the initial step. The color development is stopped and the intensity of the color is measured.

Gene ID	7508
Antigen	XPC
Tag	XPC
Usage Notes	Do not mix components from different kit lots or use reagents beyond the kit expiration date. Allow all reagents to warm to room temperature for at least 30 minutes before opening. Pre-rinse the pipet tip with reagent, use fresh pipet tips for each sample, standard and reagent to avoid contamination. Unused wells must be kept desiccated at 4 °C in the sealed bag provided. Mix Thoroughly is very important for the result. It is recommended using low frequency oscillator or slight hand shaking every 10 minutes. It is recommended that all samples and standards be assayed in duplicate or triplicate.

Applications	ELISA
Applications Notes	This Human DNA repair protein complementing XP-C cells (XPC) ELISA Kit employs a two-site sandwich ELISA to quantitate XPC in samples. An antibody specific for XPC has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyXPC present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for XPC is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of XPC bound in the initial step. The color development is stopped and the intensity of the color is measured.

Storage Instructions	The unopened kit should be stored at 2 - 8°C. After opening, please store refer to protocols.
Shipping	Gel pack with blue ice.

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