Mouse a1M(Alpha-1-Microglobulin/Bikunin Precursor) ELISA Kit

2h

200ug/mL

0.94ug/mL

Mus musculus

2.47-200ug/mL

Competitive Inhibition

Infection immunity;Immune molecule;Kidney biomarker;

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

AMBP; UTI; HCP; EDC1; HI30; IATIL; ITILC; ITI; ITIL; Alpha 1 Microglobulin/Bikunin Precursor; Growth-inhibiting protein 19; Uristatin; Uronic-Acid-Rich Protein; Trypstatin

The Mouse a1M(Alpha-1-Microglobulin/Bikunin ) ELISA Kit is a α- or alpha protein sometimes glycoprotein present in blood.Precursor cell, also called a blast cell or simply blast, is a type of partially differentiated, usually unipotent cell that has lost most or all of the stem cell multipotency.

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.

This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Alpha-1-Microglobulin/Bikunin Precursor (α1M) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Alpha-1-Microglobulin/Bikunin Precursor (α1M) and unlabeled Alpha-1-Microglobulin/Bikunin Precursor (α1M) (Standards or samples) with the pre-coated antibody specific to Alpha-1-Microglobulin/Bikunin Precursor (α1M). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Alpha-1-Microglobulin/Bikunin Precursor (α1M) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Alpha-1-Microglobulin/Bikunin Precursor (α1M) in the sample.