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Medical Consumables Accurately Detect Ovulation LH Elisa Test Kit

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Medical Consumables Accurately Detect Ovulation LH Elisa Test Kit

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Brand Name :BIOVANTION
Model Number :TY004
Certification :ISO 13485
Place of Origin :CHINA
MOQ :1 Box
Price :discussible
Payment Terms :L/C, D/A, D/P, T/T, Western Union, MoneyGram
Supply Ability :1000 Box/carton
Delivery Time :three-eigth days
Packaging Details :carton/box
Material :Serum
Format :ELISA test
Kit Size :96 Test/Kit
Brand :BIOVANTION
Exp :18 months
Storage Conditions :2-8℃
package :carton
Application :Be trying to get pregnant
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View Product Description

Result Precision HL ELISA Reagent Test Kits

Description

This product is used in laboratories, community hospitals, large hospitals, etc.One product can test 96 people, and the oper

ation is rigorous, the results are accurate, and the process is clear.100% accuracy.

Product Description
Specimen Serum
Format ELISA test
Kit Size96 Test/Kit 96 tests/box
Manufacturer BIOVANTION
Exp 18 months
Storage Conditions 2-8℃
Package carton
Application Be trying to get pregnant

Features of Hbasg Elisa Kit:
1. Sensitive
2. Accurate
3. High quality
4. Economic price

5. Reliable and Easy to Use

Medical Consumables Accurately Detect Ovulation LH Elisa Test Kit

Medical Consumables Accurately Detect Ovulation LH Elisa Test Kit

Intended use:

• Immunoassay for the in vitro quantitative determination of Hbsab in human serum.

1. 2. 3. 4. Serum and plasma samples were collected from the venous blood by conventional method. Plasma sample: add 100ul heparin solution (1%) to 5 ~ 10ml blood; or sodium citrate solution (3.8%) to plasma according to the proportion of 1:9; or EDTA solution (15%) 0.04ml to 5ml plasma. Serum and plasma samples can be stored at 4 ℃ if tests will be done within 5 days, otherwise stored at -20 ℃. No more than 3 times of freeze-thaw. Whole blood samples can be stored at 2 ℃-8 ℃ if tests will be done within 3 days.No frozen storage. The test result is invalid for hemolysis sample.

Precision
Precision was determined using reagents, pooled human sera, and controls in a modifified protocol (HL) of the CLSI (Clinical and Laboratory Standards Institute): 2 times daily for 20 days (n = 40). The following results were obtained

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