catalog number :
MBS762913
products type :
ELISA Kit
products full name :
Rat Kidney Injury Molecule 1 ELISA Kit
products short name :
[Kidney Injury Molecule 1]
products name syn :
[KIM-1 (Kidney Injury Molecule 1)/HAVCR1/HAVCR/HAVCR-1/KIM-1/KIM1/TIM/TIM-1/TIM1/TIMD-1/TIMD1]
other names :
[kidney injury molecule 1; Kidney injury molecule 1; Kidney injury molecule 1]
products gene name :
[Kim-1]
other gene names :
[havcr1]
uniprot entry name :
Q6DH50_DANRE
specificity :
This assay has high sensitivity and excellent specificity for detection of KIM-1. No significant cross-reactivity or interference between KIM-1 and analogues was observed.
storage stability :
Store at 4 degree C if kit is to be used within 1 week. Stable for 6 months (if micro ELISA Plate, Lyophilized Standard and Concentrated Biotinylated Detection Protein stored at-20 degree C. Other components at 2-8 degree C). Stable for 12 months (if the entire kit is stored at-20 degree C).
image1 heading :
Typical Testing Data/Standard Curve (for reference only)
other info1 :
Samples: Serum, Plasma, Tissue Homogenates And Other Biological Fluids. Assay Type: Sandwich. Detection Range: 0.156-10ng/ml. Sensitivity: <0.094ng/ml
other info2 :
Intra-assay Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level KIM-1 were tested 20 times on one plate, respectively. Intra-Assay: CV<8%. Inter-assay Precision: Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level KIM-1 were tested on 3 different plates, 8 replicates in each plate. CV (%) = SD/meanX100. Inter-Assay: CV<10%
products description :
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti-KIM-1 antibody was pre-coated onto 96-well plates. And the biotin conjugated anti-KIM-1 antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates 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 acc num :
ABP97434.1
ncbi mol weight :
29,575 Da
size4 :
10x96-Strip-Wells