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- 文献和实验
- 技术资料
- 保存条件:
"-20°C/-80°C"
- 保质期:
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
- 英文名:
Customized Human PDZK1IP1 Protein (in vitro E.coli)
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 规格:
20ug
Alternative Name(s)
PDZK1-interacting protein 1 Alternative name(s): 17 kDa membrane-associated protein Protein DD96Editorial/Sponsord
EditorialUniprot ID
Q13113Gene Names
PDZK1IP1Organism
HumanAASequence
MSALSLLILGLLTAVPPASCQQGLGNLQPWMQGLIAVAVFLVLVAIAFAVNHFWCQEEPE PAHMILTVGNKADGVLVGTDGRYSSMAASFRSSEHENAYENVPEEEGKVRSTPMExpression Region
1-114aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1400Purity
Greater than 85% as determined by SDS-PAGE.Storage Buffer
Tris/PBS-based buffer, 6% TrehaloseStorage
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.Endotoxin
Not Test. Endotoxin removal service is available for free upon you request.产品类型
Transmembrane-Protein备注
**产品信息可能有变动,请以官网信息为准
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文献和实验**产品信息可能有变动,请以官网信息为准
蛋白分离纯化概述(An overview of protein isolation)
chemical energy to mechanical motion. Similarly, living organisms such as the human body are complex machines made up of many interacting systems. Proteins constitute the majority of the working parts of these systems and there are thus diverse reasons
Prediction of Protein‐Protein Interaction Networks
interacting protein families are first generated along with the 16S ribosomal RNA sequence alignments for the same taxa. (B ) Distance matrices are generated from the alignments (with tree‐of‐life distances subtracted from the distance matrices in the case
Protein Interaction Cloning by Far-Western Screening of -Phage cDNA Expression Libraries
hybridization screening of cDNA libraries. This biochemical approach, however, is an enormously laborious task, and in the vast majority of cases, the yields of protein are simply inadequate to make it feasible. As an alternative, cDNAs encoding interacting
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