OxiSelect™ Aldehyde-Induced DNA Damage ELISA test kit (Ethenocytidine quantification)

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OxiSelect™ Aldehyde-Induced DNA Damage ELISA test kit (Ethenocytidine quantification)

Size

96 assays

Catalog no.

STA-821

Price

681 EUR

 

Details

This reagent is purified

0.97

Species compatible to

Humans

Use of this test kit or product

Genetics lab

Living modified organisme in this reagent or LMO

Not applicable

We send this reagant on

Room temperature

Molecular weight

in kilo Danlto or kDa

Type of reagent

Oxidative Stress/Damage

Antigen

a specific protein sequence

Group

Enzyme-Linked Immunosorbent Assay kits

Cellular use

Detect as little as 625 nM of ethenocytidine

Protocol information

Suitable for use with DNA isolated from cells or tissues

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Reagent properties

Unknown samples are compared with a provided ethenocytidine standard

Buffer

The concentration in mg/ml in a 10mM of buffered solution at pH 7 to 7,01

Related techniques

Oxidative Stress/ Damage, DNA / RNA Damage and Repair, Aldehyde Induced DNA Damage Assays, Ethenocytidine ELISA

SDS or safty data sheet

(STA-821) GHS.pdf

Technical file

kit.pdf

Description

Induced protein genes, factors or kinases, increase the production of (an enzyme or other protein) at the level of genetic transcription.

The temperatureerature for storage is

Upon receipt, store the Ethenocytidine Standard and Anti-Ethenocytidine Antibody at -20ºC. Store all other components at 4ºC until their expiration dates.

Storage

Human ELISAs or ELISA kits will be stored at +4°C. The expiry date is mostly determined by the standard stability. If your ELISA kit is expired we can supply a new standard so it will still be functional.

Use of the reagent

The OxiSelect™ Aldehyde-Induced DNA Damage ELISA test kit (Ethenocytidine quantification) is a competitive ELISA test kit allowing the quantification of ethenocytidine adducts in DNA isolated from cells or tissues. Samples and standards are added to a provided microplate preabsorbed with etheno-damaged DNA. An anti-ethenocytidine antibody is added and binds competitively to ethenocytidine in the unknown sample or to the ethenocytidine in the DNA coated on the plate. After washing a secondary antibody is added. A low signal means most of the primary antibody was bound to the unknown, indicating a high level of ethenocytidine in the sample.