
Recombinant humaan LKB1/STK11-eiwit
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
SK11 is a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Recombinant human STK11 protein, fused to His-tag at N-terminus, was expressed in E. coli.
Serine/threonine-protein kinase 11, Polarization-related protein LKB1, PJS
E.coli
Human
His-Tag
SDS-PAGE, Denatured
0.5 mg/mL (determined by Bradford assay)
> 85% by SDS-PAGE
51kDa (456aa)
STK11, STK 11, Serine/threonine-protein kinase 11, Serine/threonine-protein kinase, Polarization-related protein LKB1, Polarization related protein LKB1, PJS, LKB1, LKB 1, Hlkb1, ATGP2952-10 µg, ATGP2952-20 µg, ATGP2952-50 µg, ATGP2952-100 µg, ATGP2952-250 µg, ATGP2952-500 µg, ATGP2952-1 mg, ATGP2952-010, ATGP2952-020, ATGP2952-050, ATGP2952-100, ATGP2952-250, ATGP2952-500, ATGP2952-01M
Mack HI., et al. (2013) Virology 446 (1-2), 9-16
Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
Liquid in. 20 mM Tris-HCl buffer (pH 8.0) containing 10% glycerol
Cell Cycle
NP_000446
Q15831
Human
MGSSHHHHHH SSGLVPRGSH MGSMEVVDPQ QLGMFTEGEL MSVGMDTFIH RIDSTEVIYQ PRRKRAKLIG KYLMGDLLGE GSYGKVKEVL DSETLCRRAV KILKKKKLRR IPNGEANVKK EIQLLRRLRH KNVIQLVDVL YNEEKQKMYM VMEYCVCGMQ EMLDSVPEKR FPVCQAHGYF CQLIDGLEYL HSQGIVHKDI KPGNLLLTTG GTLKISDLGV AEALHPFAAD DTCRTSQGSP AFQPPEIANG LDTFSGFKVD IWSAGVTLYN ITTGLYPFEG DNIYKLFENI GKGSYAIPGD CGPPLSDLLK GMLEYEPAKR FSIRQIRQHS WFRKKHPPAE APVPIPPSPD TKDRWRSMTV VPYLEDLHGA DEDEDLFDIE DDIIYTQDFT VPGQVPEEEA SHNGQRRGLP KAVCMNGTEA AQLSTKSRAE GRAPNPARKA CSASSKIRRL SACKQQ
Beschrijving
SK11 is a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated
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