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公司旨在为客户提供高质量的实验外包服务（CRO服务），包括实验方案设计，常规基因工程实验操作，重组蛋白表达与纯化，重组抗体制备，天然蛋白分离与纯化，病毒分离培养等免疫学相关技术服务；同时我们也为工业客户提供部分IVD级别抗体和抗原原料。核心平台：---噬菌体抗体展示技术平台苏州蚂蚁淘生物科技有限公司利用自有的噬菌体（M13，T7噬菌体）展示技术平台，能够为客户提供极具性价比的重组Vhh抗体（纳米抗体/驼类纳米抗体）制备方案，包括动物免疫，文库建立，文库筛选以及重组抗体的体外表达等。---抗体工程技术平台卡梅德生物科技的抗体工程平台包含单克隆抗体制备服务平台，多克隆抗体制备服务平台，抗体测序与改造平台。单克隆抗体制备平台：基于杂交瘤技术的小鼠单抗技术平台，最快能够在2-3个月获得高亲和力与高特异性的单克隆抗体，同时基于噬菌体展示技术，我司能够制备多物种的重组单克隆抗体，包括小鼠，兔子，骆驼，羊驼以及人单抗。多克隆抗体制备服务平台：能够为客户提供兔多抗，羊多抗，骆驼类多抗，牛多抗等多物种的抗体制备服务，根据不同的抗原类型，来自蚂蚁淘生物的资深抗体专家会为您量身定做适合您需求的方案，以满足您的项目要求并节省您的宝贵时间。抗体一级序列测序平台：为满足大量客户对抗体基因序列与氨基酸序列信息的需求，我们为客户提供De Novo抗体全长氨基酸序列解析和N端测序服务；同时我们设计积累多达80种杂交瘤抗体基因测序引物。抗体改造技术平台：蚂蚁淘生物技术的抗体改造平台包括嵌合抗体制备，抗体亲和力成熟以及抗体人源化服务。目前我们已经成功制备十几例嵌合抗体与人源化抗体，均成功交付。---蛋白表达与纯化服务技术平台蚂蚁淘生物科技目前拥有四大蛋白表达平台，能为客户提供全面且优质的蛋白表达技术服务。哺乳动物表达平台：目前公司拥有Freestyle CHO，Expi CHO，CHO-DG44，HEK293F，Vero等细胞系用于蛋白表达制备。公司秉承质量优先原则，全部统一采用Gibco细胞培养基和相关转染配套试剂，以保证每个批次的哺乳动物细胞蛋白表达产品高质量、高表达水平的交付。同时公司拥有的表达载体体系，远高于市面常用蛋白表达载体，能够为客户提供高纯度蛋白。昆虫细胞表达平台：目前公司常采用的昆虫表达细胞为SF9，配套使用的是来自Gibco的培养基，只...
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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