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苏州蚂蚁淘生物科技有限公司SuZhouebiomall BIOLOGicalTechnologyCo.,Ltd.成立于2017年，经过数年的努力已迅速成为集科研和生产为一体的专业化生物工程公司。特别是ELISA研发，代测，技术服务这一产品已使上海抚生成为中国知名公司。公司产品涵盖ELISA研发、细胞培养，各种生化试剂、各种酶类、分子生物学试剂盒、培养基、自产实验室耗材、小型仪器等。此外、上海抚生还代理了美国药典标准品，中检所标准品，sigma,ScienCell,ATCC,wak0,omega，Worthington、MBI、Bioworld、Calendon等国外各类知名公司的产品。上海抚生将进一步加强人才经营、产品经营，不断提升企业的核心竟争力，实现具有高科技产业体系、知识化创业团队的国际化的公司，服务于生命科学领域，迎接世界经济一体化所带来的机遇与挑战。
Enzymatics是分子生物学试剂和制造服务的L先供应商，提供了无与伦比的质量，*性和价值的商业基因组科学界。该公司在美国制造商在ISO 13485认证，专注于建立长期合作伙伴关系，并利用内部和外部创新的突破性技术商业化。
详细介绍
| Product Name | Part No. | Unit Size | Concentration | Notes | |
| NEW PRODUCTS: | |||||
| E. coli DNA Ligase | L6090L | 2,500 | 10,000 U/ml | Efficiently ligates DNA at nicks and cohesive termini. Blunt-ended termini can be joined in the presence of PEG | |
| T4 RNA Ligase 2 | L6080L | 4,500 | 30,000 U/ml | Ligates nicks on double stranded DNA and from the 3′ OH of RNA to the 5′ phosphate of DNA in double stranded structures | |
| T4 RNA Ligase 2 Truncated | L6070L | 500 | 5,000 U/ml | Requires a preadenylated 5′ phosphate containing DNA or RNA to ligate to 3′ hydroxyl of RNA | |
| Omni Klentaq® | P7500-HC-L | 8,400 | 42,000 U/ml | Engineered Taq Polymerase mutant which enables PCR direct from blood, soil, water and food samples. Increased tolerance to fluorescent intercalating dyes | |
| （High Concentration） | |||||
| Omni Klentaq® | P7500-LC-L | 8,400 | 4,200 U/ml | Lower concentration – 1 microliter per reaction | |
| （Low Concentration） | |||||
| Phoenix Hot Start Taq DNA Polymerase | P7590L | 500 | 5,000 U/ml | Antibody based Hot Start Taq DNA polymerase delivers robust PCR performance with exceptional pre-PCR cycling room temperature stability | |
| VeraSeq™ 2.0 High-Fidelity DNA Polymerase | P7511L | 500 | 2,000 U/ml | Industry-leading speed, fidelity and robustness delivered via an engineered PCR polymerase | |
| VeraSeq™ ULtra DNA Polymerase | P7520L | 500 | 2,000 U/ml | High fidelity, speed, and robustness in PCR delivered by an engineered, thermostable DNA polymerase that tolerates uracil templates, nucleotides and primers | |
| RecA | Y9260L | 1.5 mg | 2.0 mg/ml | Promotes strand exchange of single-stranded DNA fragments with DNA duplex substrates | |
| Thermolabile Phosphatase | Y9210L | 5,500 | 5,000 U/ml | Removes 5′ and 3′-phosphate groups from DNA | |
| Thermolabile UDG | G5020L | 500 | 1,000 U/ml | Removes uracil from DNA, leaving AP site | |
| Poly A Polymerase | P7460L | 1,000 | 5,000 U/ml | Catalyzes the addition of AMP from ATP to the 3′ hydroxyl of RNA which is useful for making polyA tailed RNA | |
| Ultra Pure Ligases: | |||||
| Bitmap E. coli DNA Ligase | L6090L | 2,500 | 10,000 U/ml | Efficiently ligates DNA at nicks and cohesive termini. Blunt-ended termini can be joined in the presence of PEG | |
| T3 DNA Ligase | L6010L | 900,000 | 3,000,000 U/ml | Works in high ionic strength – to 1.0 M NaCl | |
| T4 DNA Ligase | L6030-LC-L | 150,000 | 120,000 U/ml | Low concentration overnight ligation format | |
| T4 DNA Ligase （Rapid） | L6030-HC-L | 240,000 | 600,000 U/ml | “Ultrapure ligase” referenced in Nature Methods （Quail, 1 December 2008） | |
| Bitmap T4 RNA Ligase 1 | L6050L | 10,000 | 20,000 U/ml | Single-stranded RNA ligase. Also joins single-stranded DNA molecules | |
| T4 RNA Ligase 2 | L6080L | 4,500 | 30,000 U/ml | Ligates nicks on double stranded DNA and from the 3′ OH of RNA to the 5′ phosphate of DNA in double stranded structures | |
| Bitmap T4 RNA Ligase 2 Truncated | L6070L | 500 | 5,000 U/ml | Requires a preadenylated 5′ phosphate containing DNA or RNA to ligate to 3′ hydroxyl of RNA | |
| T7 DNA Ligase | L6020L | 900,000 | 3,000,000 U/ml | 1000 fold higher activity on sticky ends than blunt ends | |
| Taq DNA Ligase | L6060L | 20,000 | 40,000 U/ml | Thermostable DNA ligase which efficiently seals nicks and discriminates against mismatch ligation | |
| Ultra Pure Polymerases: | |||||
| DNA Polymerase I | P7050L | 5,000 | 10,000 U/ml | DNA polymerase with 5′→ 3′ synthesis, | |
| 5′→ 3′ and 3′→ 5′ exonuclease activities | |||||
| Klenow （3′→ 5′ exo-） | P7010-HC-L | 10,000 | 50,000 U/ml | Proven choice for DNA labeling, A-tailing | |
| Klenow （3′→ 5′ exo-） | P7010-LC-L | 10,000 | 5,000 U/ml | Proven choice for DNA labeling, A-tailing | |
| Klenow Fragment | P7060L | 2,500 | 5,000 U/ml | DNA polymerase useful for end-filling prior to blunt-end ligation | |
| Mako DNA Polymerase | P7090L | 3,000 | 30,000 U/ml | Exonuclease-deficient polymerase, lacks strand displacement activity | |
| Manta 1.0 DNA Polymerase | P7140-HC-L | 100,000 | 400,000 U/ml | Thermostable Bacillus DNA Polymerase, strong strand displacement | |
| （High Concentration） | |||||
| Manta 1.0 DNA Polymerase | P7140-LC-L | 100,000 | 40,000 U/ml | Thermostable Bacillus DNA Polymerase, strong strand displacement | |
| （Low Concentration） | |||||
| Bitmap M MuLV Reverse Transcriptase | P7040L | 100,000 | 200,000 U/ml | Useful polymerase for first-strand DNA synthesis | |
| Omni Klentaq® | P7500-HC-L | 8,400 | 42,000 U/ml | Engineered Taq Polymerase mutant which enables PCR direct from blood, soil, water and food samples. Increased tolerance to fluorescent intercalating dyes | |
| Bitmap （High Concentration） | |||||
| Omni Klentaq® | P7500-LC-L | 8,400 | 4,200 U/ml | Lower concentration – 1 microliter per reaction |
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