ELISA Kit for Luteinizing Hormone Beta Polypeptide (LHb)
Sizes: 24T, 48T, 96T
Catalogue Numbers: CEC579Hu-24, CEC579Hu-48, CEC579Hu-96
Citations, Manuals and MSDS Available upon request.
Featured Series: Competitive kit
Target: Luteinizing Hormone Beta Polypeptide
Alternative Names: LH-B; CGB4; LSH-B; hLHB; Lutropin Subunit Beta; Interstitial Cell Stimulating Hormone, Beta Chain
Target Species: Human
Uniprot: P01229
Gene ID: 3972
Featured Series Function: Detects small molecule
Specificity: Reactive with Human LHb / Luteinizing Hormone Beta Polypeptide
Method: Colormetric
Detection principle: Competitive Inhibition
Detection
range: 246.91-20000pg/mL
Sensitivity: 90.4pg/mL
Assay Time: 2h
Sample Size: 50uL
Recommended/Predicted
Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids
Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12%
Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life)
Shelf-life: 12 months
Specificity: This assay has high sensitivity and excellent specificity for detection of Luteinizing Hormone Beta Polypeptide (LHb).
No significant cross-reactivity or interference between Luteinizing Hormone Beta Polypeptide (LHb) and analogues was observed.
Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Luteinizing Hormone Beta Polypeptide (LHb) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Luteinizing Hormone Beta Polypeptide (LHb) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Stability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Target: 1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
And then add 50µL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 50µL Stop Solution. Read at 450 nm immediately.
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Luteinizing Hormone Beta Polypeptide (LHb) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Luteinizing Hormone Beta Polypeptide (LHb) and unlabeled Luteinizing Hormone Beta Polypeptide (LHb) (Standards or samples) with the pre-coated antibody specific to Luteinizing Hormone Beta Polypeptide (LHb). 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 Luteinizing Hormone Beta Polypeptide (LHb) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Luteinizing Hormone Beta Polypeptide (LHb) in the sample.
Research Area: Reproductive science;
Research Use Only