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96 Wells 48 Wells Mouse Strong Specificity Cathelicidin Antimicrobial Peptide ELISA Kit

Shanghai Korain Biotech Co., Ltd
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96 Wells 48 Wells Mouse Strong Specificity Cathelicidin Antimicrobial Peptide ELISA Kit

Brand Name : BT Lab

Model Number : Cat.No E1739Mo

Certification : CE, ISO9001:2005, MSDS

Place of Origin : Shanghai, China

MOQ : Negotiation

Price : Negotiation

Payment Terms : Western Union, T/T

Supply Ability : In Stock

Delivery Time : 1-3 business days, bulk order within one week

Packaging Details : Wrapped with ice pack and styrofoam package

Discount : Available

Shipping : DHL/FedEX

Assay Length : 2 hours

Test Method : Assay Length

Bulk Order : Yes

Storage : 2-8°C

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96 Wells 48 Wells Mouse Strong Specificity Cathelicidin Antimicrobial Peptide ELISA Kit
​​
Cat.No E1739Mo
Standard Curve Range: 0.05ng/ml - 15ng/ml
Sensitivity: 0.02ng/ml
Size: 96 wells
Precision
Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision.
CV(%) = SD/mean x 100
Intra-Assay: CV<8%
Inter-Assay: CV<10%

Reagent Provided

ComponentsQuantity
Standard Solution (16ng/ml)0.5ml x1
Pre-coated ELISA Plate12 * 8 well strips x1
Standard Diluent3ml x1
Streptavidin-HRP6ml x1
Stop Solution6ml x1
Substrate Solution A6ml x1
Substrate Solution B6ml x1
Wash Buffer Concentrate (30x)20ml x1
Biotin-Conjugate Anti-Mouse cAMP/LL-37 Antibody1ml x1
User Instruction1
Plate Sealer2 pics
Zipper bag1


Specimen Collection
Serum Allow serum to clot for 10-20 minutes at room temperature. Centrifuge at 2000-3000 RPM for 20 minutes.

Plasma Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 2000-3000 RPM at 2 - 8°C within 30 minutes of collection.

Urine Collect by sterile tube. Centrifuge at 2000-3000 RPM for approximately 20 minutes. When collecting pleuroperitoneal fluid and cerebrospinal fluid, please follow the procedures above-mentioned.

Cell Culture Supernatant Collect by sterile tubes when examining secrete components. Centrifuge at 2000-3000 RPM for approximately 20 minutes. Collect the supernatants carefully. When examining the components within the cell, use PBS (pH 7.2-7.4) to dilute cell suspension to the cell concentration of approximately 1 million/ml. Damage cells through repeated freeze-thaw cycles to let out the inside components. Centrifuge at 2000-3000 RPM for approximately 20 minutes.

Tissue Rinse tissues in PBS (pH 7.4) to remove excess blood thoroughly and weigh before homogenization. Mince tissues and homogenize them in PBS (pH7.4) with a glass homogenizer on ice. Thaw at 2-8°C or freeze at -20°C. Centrifuge at 2000-3000 RPM for approximately 20 minutes.

*Sample can't be diluted with this kit. Owing to the the material we use to prepare the kit, the sample matrix interference may falsely depress the specificity and accuracy of the assay.

Reagent Preparation
All reagents should be brought to room temperature before use.
Standard Reconstitute the 120μl of the standard (16ng/ml) with 120μl of standard diluent to generate a 8ng/ml standard stock solution. Allow the standard to sit for 15 mins with gentle agitation prior to making dilutions. Prepare duplicate standard points by serially diluting the standard stock solution (8ng/ml) 1:2 with standard diluent to produce 4ng/ml, 2ng/ml, 1ng/ml and 0.5ng/ml solutions. Standard diluent serves as the zero standard(0 ng/ml). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:

8ng/mlStandard No.5120μl Original Standard + 120μl Standard Diluent
4ng/mlStandard No.4120μl Standard No.5 + 120μl Standard Diluent
2ng/mlStandard No.3120μl Standard No.4 + 120μl Standard Diluent
1ng/mlStandard No.2120μl Standard No.3 + 120μl Standard Diluent
0.5ng/mlStandard No.1120μl Standard No.2 + 120μl Standard Diluent

Standard ConcentrationStandard No.5Standard No.4Standard No.3Standard No.2Standard No.1
16ng/ml8ng/ml4ng/ml2ng/ml1ng/ml0.5ng/mll


Wash Buffer Dilute 20ml of Wash Buffer Concentrate 30x into deionized or distilled water to yield 500 ml of 1x Wash Buffer. If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved.

Summary

1. Prepare all reagents, samples and standards.

2. Add sample and ELISA reagent into each well. Incubate for 1 hour at 37°C.

3. Wash the plate 5 times.

4. Add substrate solution A and B. Incubate for 10 minutes at 37°C.

5. Add stop solution and color develops.

6. Read the OD value within 10 minutes.



































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