Human Kim-1 ELISA Kit | Kim-1 elisa kit
Kim-1 Human ELISA Kit
Reactivity
Human
Applications
ELISA
Synonyms
Kim-1; N/A; Kim-1 Human ELISA Kit; Human Kim-1; Kim-1 elisa kit
Reactivity
Human
Assay Type
Sandwich
Samples
Human serum, plasma, urine, cell culture supernatant or tissue samples
Detection Range
31.2 pg/ml-2000 pg/ml
Applicable Applications for Kim-1 elisa kit
Quantitative sELISA (EIA)
Application Notes
For quantitative detection of KIM-1 in human serum, plasma, urine, cell culture supernatant or tissue samples.
Preparation and Storage
Store at 2-8 degree C for 6 months.
Standard Curve (Sample)
Related Product Information for Kim-1 elisa kit
Background: KIM1, also known as Hepatitis A virus cellular receptor 1, is a protein that in humans is encoded by the HAVCR1 gene, which maps to 5q33.2. It is a major cause of orally transmitted acute hepatitis, infects primate cells, but not dog or rat cells, after binding to the HAV cellular receptor (HAVCR). Infection of canine osteogenic sarcoma cells expressing HAVCR1 with HAV led Feigelstock et al. (1998) to conclude that the protein is indeed a receptor for the virus. Khademi et al. (2004) found that differential expression of TIMs by Th1 and Th2 cells may be implicated in different phases of an autoimmune disease.
Principle of the Assay: This kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. The purified anti-KIM-1 antibody was pre-coated onto 96-well plates. And the HRP conjugated anti-KIM-1 antibody was used as detection antibodies. The standards, test samples and HRP conjugated detection antibody were added to the wells subsequently, mixed and incubated, then, unbound conjugates were washed away with wash buffer. TMB substrates (A & B) were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the KIM-1 amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of KIM-1 can be calculated.
Principle of the Assay: This kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. The purified anti-KIM-1 antibody was pre-coated onto 96-well plates. And the HRP conjugated anti-KIM-1 antibody was used as detection antibodies. The standards, test samples and HRP conjugated detection antibody were added to the wells subsequently, mixed and incubated, then, unbound conjugates were washed away with wash buffer. TMB substrates (A & B) were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the KIM-1 amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of KIM-1 can be calculated.
NCBI and Uniprot Product Information
NCBI GI #
NCBI Official Full Name
kidney injury molecule-1
