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120 Minutes ISO13485 Syphilis Elisa Test Kit TP Elisa 96 Tests Kit

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120 Minutes ISO13485 Syphilis Elisa Test Kit TP Elisa 96 Tests Kit

Country/Region china
City & Province beijing beijing
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Product Details

Hot Sale Syphilis Elisa Kit (TP Elisa Kit) 96 Tests/Kit
Catalog No.: BE801A
For the detection of Total Antibody to Treponema Pallidum in human serum or plasma (in vitro) .

1. INTENDED USE

The Anti-TP ELISA is a qualitative enzyme immunoassay for the in vitro detection of Treponema Pallidum (TP) infection, based on the detection of total antibody to Treponema Pallidum in human serum or plasma. It is intended for screening of blood donors and diagnosing patients related to infection with TP.

 

2.COMPONENTS

Materials provided with the kits:

ItemDescription96T
1Microtiter Well1
2Negative Control1ml
3Positive Control1ml
4Sample Diluent6ml
5Conjugate12ml
6Washing Buffer (20×)40ml
7Substrate Solution A6ml
8Substrate Solution B6ml
9Stop Solution6ml
10Plate Cover3pieces
11Insert1 copy

 

3.ASSAY PROCEDURE 

  1. Prepare Reagents: Dilute 1 volume of Concentrated Washing Buffer (20×)with 19 volumes of distilled water, mix well.
  2. Add Samples: Open the foil pouch and remove the Microplate. Set up 1 well as Blank, 2 wells as negative control, 2 wells as positive control. After dispensing 50μL of Sample Diluent , dispense 50μL of sample or negative control or positive control to the respective wells. Gently vibrating the plate.
  3. Incubate: Cover the Microplate with plate cover and incubate the Coated Microplate in a thermostat-controlled water-bath or microplate incubator at 37℃ for 60 minutes.
  4. Wash the Plate: Remove the plate cover. Aspirate the contents of all wells. Fill the wells with the diluted washing buffer ( 10~20 seconds to soak) then aspirate again. Repeat the procedure for 5 times. Make sure that the rest volume is minimal, by tapping plate onto absorbent paper.
  5. Add Conjugate: Add 100μL of conjugate to each well (except for the blank well).
  6. Incubate: Cover the Microplate and incubate the plate at 37℃ for 30 minutes.
  7. Wash the Plate: Repeat the wash procedure as in step 4.
  8. Add Substrate: Add 50μL of Substrate Solution A and 50μL of Substrate Solution B to each well, mix well. Cover and incubate at 37℃ for 30 minutes.
  9. Stop reaction: Add 50μL Stop Solution to each well, mix well.
  10. Read the absorbance at 450 nm. If a dual wavelength measurement is used, the reference wavelength should be selected from 620nm to 690nm.

 

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