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| # | Company | Amount | Rank | Status |
|---|---|---|---|---|
| 1 | L2₹40,610−₹2,590 (5.88%)Accepted-AOC 32 42 R EB COLONY KENDAIYUR ROAD METTUPALAYAM COIMBATORE TAMIL NADU 641305 | COIMBATORE | TAMIL NADU | 641305 | ₹40,610−₹2,590 (5.88%) Quoted ₹41,440 | L2 | Accepted-AOC Accepted |
| 2 | L1₹44,030Rejected-AOC 7 17 BALAKRISHNAPURAM 2ND STREET ADAMBAKKAM KANCHIPURAM TAMIL NADU 600088 | CHENNAI | TAMIL NADU | 600088 | ₹44,030 | L1 | Rejected-AOC Rejected |
| 3 | Rejected-Technical | - | - | Rejected-Technical Rejected |
| Sl No | Description | Qty | Unit | Synergy Scientific Services Private Limited L2 | PRIORITY LIFESCIENCE L1 |
|---|---|---|---|---|---|
| 1.00Purchase of Chemicals | |||||
| 1.01 | In-Fusion® Snap Assembly Master Mix Specifications:
1. Subcloning is unnecessary: clone any insert directly into your final vector, regardless of your
2. cloning locus
Highly efficient: over 95% efficiency demonstrated with a broad range of fragment sizes, from 0.5 kb to 34 kb*
3. Seamless construction: final constructs have no extra base pairs left over (as is often the case with restriction digest or TA cloning)
4. Flexible experimental design: clone single or multiple DNA fragments simultaneously, with just a single reaction
5. Mainly used for PCR cloning, High-throughput cloning, Multiple-fragment cloning, Site-directed mutagenesis, Gene synthesis, Adding adaptors, linkers, and protein tags, Cloning using modular parts | 2 | No | 22,015 ₹44,030 | 20,720 ₹41,440 Lowest |
Tender Value
Refer Docs
EMD Value
₹1,255
Closing Date
25 Jun 2026, 3:00 pmClosed
The Registrar
Bharathiar University, Coimbatore
Chemicals
2026_HE_680285_1
C7/CRTD/MBT/CMRG/CG/280
Open Tender
Chemicals
Supply
Bharathiar University
Please refer Tender documents.
8 documents required · 8 mandatory
₹0
₹1,255
Yes
18 Aug 2026
10 Jun 2026
26 Jun 2026
10 Jun 2026
25 Jun 2026
10 Jun 2026
| Sl No | Description | Qty | Unit | Est. Rate | Est. Amount |
|---|---|---|---|---|---|
| 1Purchase of Chemicals | |||||
| 1.01 | In-Fusion® Snap Assembly Master Mix Specifications:
1. Subcloning is unnecessary: clone any insert directly into your final vector, regardless of your
2. cloning locus
Highly efficient: over 95% efficiency demonstrated with a broad range of fragment sizes, from 0.5 kb to 34 kb*
3. Seamless construction: final constructs have no extra base pairs left over (as is often the case with restriction digest or TA cloning)
4. Flexible experimental design: clone single or multiple DNA fragments simultaneously, with just a single reaction
5. Mainly used for PCR cloning, High-throughput cloning, Multiple-fragment cloning, Site-directed mutagenesis, Gene synthesis, Adding adaptors, linkers, and protein tags, Cloning using modular parts | 2 | No | 100 | ₹200 |
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