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CITEST DIAGNOSTICS INC.

  • China,Hangzhou ,Zhejiang
  • Verified Supplier

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China WB S P Tetanus Toxoid Antibody Test Kit 10 Min Infectious Disease Test Kit
China WB S P Tetanus Toxoid Antibody Test Kit 10 Min Infectious Disease Test Kit

  1. China WB S P Tetanus Toxoid Antibody Test Kit 10 Min Infectious Disease Test Kit

WB S P Tetanus Toxoid Antibody Test Kit 10 Min Infectious Disease Test Kit

  1. MOQ: N/A
  2. Price: Negotiation
  3. Get Latest Price
Supply Ability 10 M tests/month
Packaging Details 40 T
Product Tetanus Rapid Test,detection of antibodies to Tetanus toxin in WB/S/P,Tetanus toxin infection
Cat. No. ITE-402
Principle Chromatographic Immunoassay
Format Cassette
Specimen WB/S/P
Certificate CE
Reading Time 10 minutes
Pack 40 T
Storage Temperature 2-30°C
Shelf Life 2 Years
Features 1 Fast results
Features 2 Easy visually interpretation
Features 3 Simple operation, no equipment required
Features 4 High accuracy
Brand Name Citest
Model Number ITE-402
Certification CE
Place of Origin -

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  1. Product Details
  2. Company Details

Product Specification

Supply Ability 10 M tests/month Packaging Details 40 T
Product Tetanus Rapid Test,detection of antibodies to Tetanus toxin in WB/S/P,Tetanus toxin infection Cat. No. ITE-402
Principle Chromatographic Immunoassay Format Cassette
Specimen WB/S/P Certificate CE
Reading Time 10 minutes Pack 40 T
Storage Temperature 2-30°C Shelf Life 2 Years
Features 1 Fast results Features 2 Easy visually interpretation
Features 3 Simple operation, no equipment required Features 4 High accuracy
Brand Name Citest Model Number ITE-402
Certification CE Place of Origin -
High Light WB S P Tetanus Toxoid Antibody TestTetanus Toxoid Antibody Test Kit 10MinTetanus Infectious Disease Test Kit
Principle Chromatographic Immunoassay
Format Cassette
Specimen WB/S/P
Certificate CE
Reading Time 10 minutes
Pack 40 T
Storage Temperature 2-30°C
Shelf Life 2 Years

 

 

Tetanus Rapid Test,detection of antibodies to Tetanus toxin in WB/S/P,Tetanus toxin infection

 

Applications: 

 

TETANUS is an immunochromatographic rapid test for semi-quantitative detection of anti tetanus toxin antibodies in serum,  plasma or  human whole blood.TETANUS is intended  for professional  use within  the framework of laboratory analysis or point of care analysis to detect immunity to tetanus toxin.

 

Description: 

   

Clostridium tetani is a bacterium that causes tetanus in humans. Clostridium tetani ate Gram-positive, spore-forming rods that are anaerobic. If they enter the body through a wound, they can multiply and produce a toxin that affects the nerves and controls the activity of muscles. Toxin of Clostridium tetani binds to membranes of peripheric nervous cells and inhibits the release of neurotransmitters.

 

Antibodies to tetanus toxin are produced in the human by the injection of chemically inactivated tetanus toxin (tetanus toxoid). Immunization is the best way to prevent C. Tetani infections in children and adults. Moreover, injection of specific and purified anti tetanus toxin IgG is used in order to refrain toxin action during an acute infection.

 

It is sometimes better to know the level of anti tetanus toxin antibodies in a patient, to evaluate their immune status, in order to determine the necessity of a complementary vaccination which would assure immunity towards tetanus toxin.

 

In emergency situations, it is important for the clinician to know the immune status in order to decide on the correct anti-tetanus prophylaxis for high risk patients (deep wounds).

 

How to use? 

Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.

  1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it as soon as possible.
  2. Place the cassette on a clean and level surface.

For Serum or Plasma specimen:

  • Hold the dropper vertically and transfer 1 drop of serum or plasma (approximately 25 mL) to the specimen well of test cassette, then add 3 drops of buffer (approximately 120ul), and start the timer. See illustration below.

For Venipuncture Whole Blood specimen:

  • Hold the dropper vertically and transfer 1 drop of whole blood (approximately 25 mL) to the specimen well, then add 3 drops of buffer (approximately120 mL), and start the timer. See illustration below.                                                   3.Wait for the colored line(s) to appear. Read results at 10 minutes.  Do not interpret the result after 20 minutes

 

INTERPRETATION OF RESULTS

(Please refer to the illustration above)

 

POSITIVE:* Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the test region (T). Sample is considered positive with an antibody level above 0.1 IU/ml.

 

*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of Tetanus antibody present in the specimen. Therefore, any shade of color in the test region (T) should be considered positive.

 

NEGATIVE: One colored line appears in the control region (C). No apparent colored line appears in the test region (T). (with anti  tetanus antibody  level below  0.1 IU/ml).

 

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test cassette. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

 

Order Information

 

Cat. No. Product Description Specimen Format Kit Size Cut-Off Status
ITE-402 Teanus Rapid Test Cassette WB/S/P Cassette 40 T See Insert CE
 

 

Company Details

Bronze Gleitlager

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Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer,Exporter,Trading Company

  • Total Annual:

    80000000-100000000

  • Employee Number:

    500~10000

  • Ecer Certification:

    Verified Supplier

CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ... CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ...

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  • CITEST DIAGNOSTICS INC.
  • 170-422, Richards Street, Vancouver BC V6B 2Z4, CANADA
  • https://www.citesttestkit.com/

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