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Oct-05-22

Toxo Igm Genlisa Elisa

$30
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The Toxoplasma gondii IgM GENLISA ELISA is intended for the qualitative determination of Toxoplasma gondii IgM antibody in human serum and plasma.

Pack Size - ELISA 96 wells
Oct-05-22

Rubella Igm Genlisa Elisa

$30
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The Rubella IgM GENLISATM ELISA is intended for the qualitative determination of Rubella Virus IgM class antibodies in human serum and plasma.

Pack Size - ELISA 96 wells
Oct-05-22

Rubella Igg Genlisa Elisa

$9
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The Rubella IgG GENLISATM ELISA is intended for the qualitative determination of Rubella Virus IgG class antibodies in human serum and plasma.

ELISA 96 wells
Oct-05-22

Hsv 1/2 Igg Genlisa Elisa

$30
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The HSV 1 & 2 IgG GENLISA ELISA is intended for the qualitative determination of HSV 1 & 2 IgG in human serum and plasma.

Pack Size - ELISA 96 wells
Oct-05-22

Hsv 1 Igm Genlisa Elisa

$30
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The HSV 1 IgM GENLISA ELISA is intended for the qualitative determination of HSV 1 IgM in human serum and plasma.
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Oct-05-22

Hsv 1 Igg Genlisa Elisa

$30
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The HSV 1 IgG GENLISA ELISA is intended for the qualitative determination of HSV 1 IgG in human serum and plasma.

Pack Size - ELISA 96 wells
Oct-05-22

Cmv Igm Genlisa Elisa

$30
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The CMV IgM GENLISA ELISA is intended for the qualitative determination of CMV IgM in human serum and plasma.

ELISA 96 wells
Oct-04-22
Supplier From Mumbai, Maharashtra, India
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The Varicella-Zoster Virus (VZV) IgM ELISA is intended for the qualitative determination of IgM class antibodies against Varicella-Zoster Virus (VZV) in human serum or plasma (citrate, heparin).

ELISA 96 wells
Oct-04-22
Supplier From Mumbai, Maharashtra, India
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The Varicella-Zoster Virus (VZV) IgG ELISA is intended for the qualitative determination of IgG class antibodies against Varicella-Zoster Virus (VZV) in human serum or plasma (citrate, heparin).
Oct-04-22

Hev Igm Genlisa Elisa

$46.45
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
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The HEV IgM GENLISA ELISA is intended for the qualitative determination of Hepatitis E Virus IgM in human serum and plasma.
Aug-05-22

Hcg Test Kit

$1
MOQ: Not Specified
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Product Name
Human Chorionic Gonadotropin (HCG) Test Kit (Immunofluorescence Chromatography)

Purpose
To detect the content of HCG in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.

Principles of Detection
The HCG Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HCG antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HCG antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody).

HCG concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HCG according to the preset calibration curve in the machine and display the result, detection unit is mIU/mL. C line should appear in any cases, which indicates the reaction system is effective.

Storage conditions and shelf life
Store in a sealed aluminum foil bag at 2 - 30 C. After unpacking the aluminum foil bag under temperature 20~30 C , humidity 35~65%, please use it immediately.
Shelf life 18 months.

Applicable instrument
Avid fluorescent immunoanalyzer model: AI-IF 600
Aug-05-22
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Product Name
Triiodothyronine (T3) Test Kit (Immunofluorescence Chromatography)

Purpose
To detect the content of T3 in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.

Principles of Detection
The T3 Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing T3 antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another T3 antigen, and the C line is pre-coated with a control line antibody (chicken IgY antibody).

T3 concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of T3 according to the preset calibration curve in the machine and display the result, detection unit is nmol/mL. C line should appear in any cases, which indicates the reaction system is effective.

Storage conditions and shelf life
Store in a sealed aluminum foil bag at 2~30�°C. After unpacking the aluminum foil bag under temperature 20~30 �ºC , humidity 35~65%, please use it immediately.
Shelf life 18 months.

Reference range
Reference value:The 95% concentrations of T3 in 239 non-stationary subjects without any obvious thyroid dysfunction ranged from 1.34 to 2.73nmol/L, with a median of 1.81nmol/L;The reference value has been verified with reference to similar products already on the market. Each laboratory can build own reference range according to actual situation.
Aug-05-22
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Product Name
C-reactive Protein(CRP)Test Kit (Immunofluorescence Chromatography)

Purpose
To detect the content of CRP in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.

Principles of Detection
The CRP Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing CRP antibody conjugated with fluorescent microspheres and a control antibody (goat anti-rabbit IgG antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another CRP antibody, and the C line is pre-coated with a control line antibody (rabbit IgG antibody).

CRP concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of CRP according to the preset calibration curve in the machine and display the result, detection unit is mg/L. C line should appear in any cases, which indicates the reaction system is effective.

Reference range
Reference values:
Aug-05-22
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Product Name
Glycosylated Hemoglobin(HbA1c)Test Kit (Immunofluorescence Chromatography)

Purpose
To detect the content of HbA1c in human whole blood in vitro quantitatively.For Professional Use only.

Principles of Detection
The HbA1c Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HbA1c antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HbA1c antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody).

HbA1c concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HbA1c according to the preset calibration curve in the machine and display the result, detection unit is %units. C line should appear in any cases, which indicates the reaction system is effective.

Storage conditions and shelf life
Store in a sealed aluminum foil bag at 2~30�°C. After unpacking the aluminum foil bag under temperature 20~30 �ºC , humidity 35~65%, please use it immediately.
Shelf life 18 months.

Applicable instrument
Avid fluorescent immunoanalyzer model: AI-IF 600
Manufacturer& After-Sales Company: Shenzhen Aivd Biotechnology Co., LTD.
Address:C501,Building B5,China Merchants Guangming Science Park, #3009 Guanguang Road, Guangming District, Shenzhen,Guangdong Province, China
Tel: 0755-26165742 Fax:0755-26401805

Specimen collection and preparation
1. Human whole blood samples can be used for this test.
2. Specimen collection:Collect blood specimen into a collection tube containing EDTA , evenly mixed before use. Do not use hemolyzed blood for testing.
Whole blood specimens should be stored at 2-8�°C for no more than 4 hours if not test immediately.
3. Do not test patients' samples with severe hemolysis, lipemia and jaundice, all specimens should be treated as infectant.
4. Restore the specimen to 20-30�°C before the detection, cryopreserved specimen should be completely thawed, rewarmed and evenly mixed before use.

Reference range
Positive: reading value â?¥6%, a positive result.
Negative: reading value 8%, poorly controlled blood glucose.
The reference value is verified with reference to similar products that have been marketed. Due to ethnic and geographical differences, each laboratory can establish its own reference interval according to the actual situation.
Mar-25-20
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Sensor De Temperatura Corporal Thermopile MTP10-B7F55 Pistola De Frente Disponible , Covid 19 corona virus test kit ( fortitude 2.0 kit nfih001 from singapore), surgical mask, military connectors ,Sullins connector for Burn-in Test, Programmable Power Supply, Adam condom, led IP67 lighting, Omron servo cables harness, Panasonic Servo cable harness
Sep-03-21

Genbody Self Test Kits

$24.70
MOQ: Not Specified
Supplier From Taipei, Taiwan
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If anyone is looking for Genbody Self Test Kits and nitrile gloves, please get in touch. Direct from Korea.
Feb-10-22
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Cellife Home Test Exw
Cellife home test is approved by Australia TGA Standard
Order: 50% deposit/balance Exw
Lead time: around 7-10days
Sometimes will have Extra OTG China
You can got the approval for sale in Australia
And Cellife distributor (none sole) in Australia will help you to Customs clearance
Feb-10-22

Flowflex Home Test Kit

$5 - $8
MOQ: Not Specified
 Inquire Now  
***FOR USA BASED END-CLIENTS ONLY***
300 PER CASE; 20 CASES / 6,000 PER PALLET; 40 X 48 72 280kgs
Bulk orders placed this week will start to deliver on/about early March with partial weekly shipments.

*Terms of sale reflect those of ACON LABS; 50% deposit; balance when goods are ready to start shipping from LA
*Full pre-payment will move you up to the front and expedite quicker shipment considerations.
* Delivery is subject to final confirmation
Jan-08-22

Covid19 Self Testing Kits

$0.75
MOQ: Not Specified
Supplier From Beijing, , China
 Inquire Now  
dear my friend, we are from Lepu Medical, the manufacturer for the self testing kits.
we are offering the goods will CE and also very fast production time.
Starting from the IVD test, our products now is hot welcomed in the world.
You may freely contact with us in the WhatsApp 008613230113351
or maybe the email address at dannis.wen@lepu-medical.com
we are opening for the worldwide buyers to have the goods.
If you need, you can also find our in our web or Alibaba.
We are willing to meet and make new friends around the world.
Dec-06-21

2019-Ncov Antigen Test Kit

$2.50
MOQ: Not Specified
Supplier From Phnom Penh, Cambodia
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This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from
human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens.
This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical
reference only and cannot be used as the sole basis for diagnosis and exclusion
decision. The clinical diagnosis and treatment of patients should be considered in
combination with their symptoms/signs, medical history, other laboratory tests and
treatment responses.
Positive test result needs to be further confirmed, negative result does not preclude
2019-nCoV infection.
This kit is intended for use by qualified and trained clinical laboratory personnel
specifically instructed and trained in the techniques of in vitro diagnostic procedures.
TEST PRINCIPLE
The kit is immunochromatographic and uses double-antibody sandwich method to
detect 2019-nCoV N protein antigen. During detection, the treated specimens are
loaded into the sample wells of the test card. When the concentration of 2019-nCoV
antigen in specimen is higher than the minimum detection limit, the viral antigen will
form complexes with labeled antibodies first. Under chromatography, the complexes
move forward along the nitrocellulose membrane till captured by pre-coated
monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to
form a pink/purple reaction line on the detection zone, at this point the result is
positive; conversely, if there is no viral antigen or the concentration of antigen in
specimen is below the minimum detection limit, no pink/purple reaction line appears
in the detection zone, at this point the result is negative. Regardless of whether the
sample contains viral antigens or not, a pink/purple reaction line will appear in the
quality control zone (C), the pink/purple reaction line that appears in the quality
control zone (C) is the criterion for determining if the chromatography process is
normal.
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