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Tender For Consumable Items For Department Of Pathology And Lab Medicine, raebareli-Uttar Pradesh

All India Institute Of Medical Sciences-AIIMS has published Tender For Consumable Items For Department Of Pathology And Lab Medicine. Submission Date for this Tender is 18-11-2022. Indicators and Reagents Tenders in raebareli Uttar Pradesh. Bidders can get complete Tender details and download the document.




Tender Notice

34736705
Tender For Consumable Items For Department Of Pathology And Lab Medicine
Open Tender
Indian
Uttar Pradesh
raebareli
18-11-2022

Tender Details

Consumable Items For Department Of Pathology And Lab Medicine , Consumable Items , Qubittmdsdnabr Assay Kits Use With Qubit Fluorometer And Quantification Raage-4-2000Ng For 100 Reaction , Qubittm Rna High Sensitivity (Hs),Assay Kits Use With Qubit Fluorometer And Quantification Raage-2-200 Ng For 100 Reaction , Qubittmassay Tubes(0.5Ml) , • Bcr-Abl 1 Rt-Pcr Kit For Detection Of Bcr-Abl 1P 210 And P190 Using Real Time Pcr-With • Both The Transcript Should Be Not Detected In Same Reaction. • Is-Mmr Calibrator Should Be Included In A Separate Vial With The Kit • Kit Should Contain High Positive And Low Positive Control • Cdna Conversion Reagent Should Be Designed According To Europe Against Cancer (Eac) Recommendation • The Kit Should Have Optimal Quality Control And Iso 13485 Standardized

Key Value

Document Fees
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EMD
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Tender Value
INR 2.50 Lakhs /-

BOQ Items

Name of Work: Purchasing of Consumable items for Department of Pathology and Lab Medicine.
Sl. No. Item Description
1Consumable Items
2QubitTMdsDNABR Assay Kits use with qubit fluorometer and quantification raage-4-2000ng for 100 reaction
3QubitTM RNA High Sensitivity (HS),Assay Kits use with qubit fluorometer and quantification raage-2-200 ng for 100 reaction
4QubitTMAssay Tubes(0.5ml)
5• BCR-ABL 1 RT-PCR kit for detection of BCR-ABL 1p 210 and p190 using real time PCR-with • Both the transcript should be not detected in same reaction. • IS-MMR calibrator should be included in a separate vial with the kit • Kit should contain high positive and low positive control • cDNA conversion reagent should be designed according to Europe Against cancer (EAC) recommendation • The kit should have optimal quality control and ISO 13485 standardized
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