上海金畔生物科技有限公司代理New England Biolabs（NEB）酶试剂全线产品，欢迎访问官网了解更多产品信息和订购。
cAMP-dependent Protein Kinase (PKA), catalytic subunit
The catalytic subunit of cAMP-dependent Protein Kinase (PKA) is a serine/threonine protein kinase. The recognition motif for phosphorylation by PKA is RRXS/TY, where Y tends to be a hydrophobic residue.
- Recombinant enzyme with no detectable protease or phosphatase contaminating activities
- Optimal activity and stability for up to 12 months
Casein Kinase II (CK2) |NEB酶试剂 New England Biolabs
上海金畔生物科技有限公司代理New England Biolabs（NEB）酶试剂全线产品，欢迎访问官网了解更多产品信息和订购。
Casein Kinase II (CK2)
Casein Kinase II (CKII) is a constitutively active serine/threonine protein kinase composed of two 44 kDa catalytic α-subunits and two 26 kDa regulatory β-subunits in an α2β2 configuration to form stable heterotetramers. The general recognition motif for phsophorylation by CKII is SXXE/D.
- Recombinant enzyme with no detectable protease or phosphatase contaminating activities
- Optimal activity and stability for up to 12 months
5-hydroxymethyluridine DNA Kinase |NEB酶试剂 New England Biolabs
上海金畔生物科技有限公司代理New England Biolabs（NEB）酶试剂全线产品，欢迎访问官网了解更多产品信息和订购。
5-hydroxymethyluridine DNA Kinase
- 5-hydroxymethyluridine DNA Kinase (5-HMUDK) transfers the gamma phosphate from ATP to the hydroxymethyl moiety of 5-hydroxymethyluridine in polymeric DNA
- This is an Enzyme for Innovation (EFI). EFI is a project initiated by NEB to provide unique enzymes to the scientific community in the hopes of enabling the discovery of new and innovative applications. These enzymes have interesting properties and unique specificities.
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JBScreen Kinase 1 – 4 CS-135 JBScreen Kinase HTS CS-204L
Jena Bioscience在结构学研究方面全面提供晶体筛选试剂盒、优化试剂、工具和各类耗材
JBScreen Kinase 1 CS-131
JBScreen Kinase 2 CS-132
JBScreen Kinase 3 CS-133
JBScreen Kinase 4 CS-134
JBScreen Kinase 1 – 4 CS-135
JBScreen Kinase HTS CS-204L
JBScreen Kinase is a highly specialized screen formulated for the determination of initial crystallization conditions of protein kinases.
Through the use of advanced data mining, crystallization conditions of kinases have been identified from published structures. Data evaluation and verification resulted in the formulation of 96 unique reagents, highly effective for the crystallization of kinases.
JBScreen Kinase utilizes a variety of different precipitating agents, i.e. various molecular weight PEGs, MPD and Ammonium Sulfate, in combination with buffers covering a pH range from 3,1 – 10,0 and numerous additives.
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