Mouse DNASE1(Deoxyribonuclease I) ELISA Kit

Order Mouse DNASE1 Deoxyribonuclease I ELISA Kit 01017454914 at Gentaur DNASE1(Deoxyribonuclease I)

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Mouse DNASE1(Deoxyribonuclease I) ELISA Kit

Size

96T

Catalog no.

ELK3360

Price

608 EUR

 

Details

Assay length

3h

Standard

80ng/mL

Assay Type

Sandwich

Sensitivity

0.51ng/mL

Latin name

Mus musculus

Detection range

1.25-80ng/mL

Research Area

Enzyme & Kinase;Developmental science;

Alternative Names

DNaseI; DNL1; DRNI; DNase-I; Dornase alfa

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED,Mouse or mice from the Mus musculus species are used for production of mouse monoclonal antibodies or mabs and as research model for humans in your lab. Mouse are mature after 40 days for females and 55 days for males. The female mice are pregnant only 20 days and can give birth to 10 litters of 6-8 mice a year. Transgenic, knock-out, congenic and inbread strains are known for C57BL/6, A/J, BALB/c, SCID while the CD-1 is outbred as strain.

Test principle

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 Deoxyribonuclease I (DNASE1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Deoxyribonuclease I (DNASE1). 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 Deoxyribonuclease I (DNASE1), 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 Deoxyribonuclease I (DNASE1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.