|Detection range||31.25-2000 pg/mL|
|Sample type &Sample volume||serum, plasma and other biological fluids; 100μL|
|Specificity||This kit recognizes Human HGF in samples. No significant cross-reactivity or interference between Human HGF and analogues was observed.|
|Reproducibility||Both intra-CV and inter-CV are < 15%.|
|Application||This CLIA kit applies to the in vitro quantitative determination of Human HGF concentrations in serum, plasma and other biological fluids.|
|Micro CLIA Plate(Dismountable)||96T: 8 wells ×12 strips
48T: 8 wells ×6 strips
|-20℃, 6 months|
|Reference Standard||96T: 2 vials
48T: 1 vial
|Concentrated Biotinylated Detection Ab (100×)||96T: 1 vial, 120 μL
48T: 1 vial, 60 μL
|Concentrated HRP Conjugate (100×)||96T: 1 vial, 120 μL
48T: 1 vial, 60 μL
|-20℃(Protect from light), 6 months|
|Reference Standard & Sample Diluent||1 vial, 20 mL||2-8°C, 6 months|
|Biotinylated Detection Ab Diluent||1 vial, 14 mL|
|HRP Conjugate Diluent||1 vial, 14 mL|
|Concentrated Wash Buffer (25×)||1 vial, 30 mL|
|Substrate Reagent A||1 vial, 5 mL||2-8℃(Protect from light)|
|Substrate Reagent B||1 vial, 5 mL|
|Plate Sealer||5 pieces|
|Certificate of Analysis||1 copy|
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Human HGF were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Human HGF were tested on 3 different plates, 20 replicates in each plate.
|Intra-assay Precision||Inter-assay Precision|
The recovery of Human HGF spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
|Sample Type||Range (%)||Average Recovery (%)|
|Cell culture media(n=8)||91-108||99|
Samples were spiked with high concentrations of Human HGF and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.
|Synonyms||F-TCF, HGFB, HPTA, SF, Scatter Factor, Hepapoietin A|
1.Add 100 μL of standard or sample to each well. Incubate for 90 min at 37℃.
2.Remove the liquid.
3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃. Aspirate and wash 3 times.
4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃. Aspirate and wash 5 times.
5.Add 100 μL Substrate Mixture Solution. Incubate for 5 min at 37℃.
6.Fluorescence appeared. Measure the RLU value with the Chemiluminescence immunoassay analyzer. Calculation of the results.
|E-ELIR-001||ELISA Plate Coating Buffer(1×)||100mL, 1000mL|
|E-ELIR-002||ELISA Plate Coating Buffer(5×)||100mL, 1000mL|
|E-ELIR-003||ELISA Plate Blocking Buffer||100mL, 1000mL|
|E-ELIR-004||Wash Buffer for Sandwich-ELISA(25×)||100mL, 1000mL|
|E-ELIR-005||Wash Buffer for Competitive-ELISA(25×)||100mL, 1000mL|
|E-ELIR-006||Stop Solution||100mL, 1000mL|
|E-ELIR-007||HRP-conjugate Stabilizer||10mL, 100mL, 500mL|
|E-ELIR-008||HRP-conjugate Diluent||100mL, 1000mL|
|E-ELIR-009||Biotinylated Antibody Stabilizer||10mL, 100mL, 500mL|
|E-ELIR-0010||Biotinylated Antibody Diluent||10mL, 100mL, 500mL|
|E-ELIR-0011||Sample Diluent||10mL, 100mL, 500mL|
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