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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20℃
- 保质期:
12个月
- 英文名:
Recombinant Deoxyhypusine Synthase (DHPS)
- 库存:
1000
- 供应商:
上海信裕
| Organism species | Mus musculus (Mouse) |
| Product No. | |
| Source | Prokaryotic expression |
| Host | E.coli |
| Purity | > 95% |
| UOM | 50ug |
| Predicted Molecular Mass | 44.3kDa |
| Concentration | n/a |
| Applications | SDS-PAGE; WB; ELISA; IP. |
| Endotoxin Level | <1.0EU per 1µg (determined by the LAL method) |
| Residues | Met1~Asp369 with two N-terminal Tags, His-tag and T7-tag |
| Formulation | Supplied as lyophilized form in 20mM Tris, 150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT, 0.01% sarcosyl, 5% trehalose, and preservative. |
MEGTPPGAAP SSALAAVLKH SSALPPESAQ VQGYDFNRGV DYHALLDAYR TTGFQATNFG RAVQQVNAMI EKKLEPLAVD EDHHADLTQS RRPLTGCTIF LGYTSNLISS GIRETIRYLV QHNMVDVLVT TAGGVEEDLI KCLAPTYLGE FSLRGKELRE SGINRIGNLL VPNDNYCKFE DWLMPILDQM VLEQNTEGVK WTPSKMISRL GKEINNPDSV YYWAHKNHIP VLSPALTDGS LGDMIFFHSY KNPGLVLDIV EDLRLINTQA IFAKRSGMII LGGGVVKHHI ANANLMRNGA DYAVYINTAQ EFDGSDSGAR PDEAVSWGKI RMDAQPVKVY ADASLVFPLL VAETFAQKAD AFRAEKNED
Stability Test: The thermal stability is described by the loss rate of the target protein. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37oC for 48h, and no obvious degradation and precipitation were observed. (Referring from China Biological Products Standard, which was calculated by the Arrhenius equation.) The loss of this protein is less than 5% within the expiration date under appropriate storage condition.
Protein bands: 10kDa, 14kDa, 18kDa, 22kDa, 26kDa, 33kDa, 44kDa and 70kDa.
Double intensity bands: The 26kDa, 18kDa, 10kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy.
Ready-to-use: No need to heat, dilute or add reducing agents before use.
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文献和实验牢记N端法则:当N端第二个残基是Leu、Arg、Lys、Phe、Tyr和Trp时,重组蛋白半衰期只有2分钟,而小侧链的氨基酸残基,如Ala,则可以提高蛋白稳定性。因此在设计载体时,要特别注意第二个密码子,避免上述残基的出现。处理高毒性蛋白:毒性极高的重组蛋白,其本底表达就会杀死原核宿主,质粒容易丢失,使其在大肠杆菌中很难得到高表达。采用可表达T7溶菌酶的宿主。T7溶菌酶是T7RNA聚合酶的抑制剂,采用含有T7溶菌酶质粒的宿主,如pLysS,可以降低重组蛋白在大肠杆菌快速生长期的本底
X-100或脱氧胆酸钠)和低浓度变性剂(2mol/L尿素或盐酸胍等)洗涤除去脂类和膜蛋白,这一步很重要,否则会导致包涵体溶解和复性的过程中重组蛋白质的降解[6、7、8]。 包涵体的溶解必须用很强的变性剂,如8mol/L尿素、6~8mol/L盐酸胍,通过离子间的相互作用破坏包涵体蛋白间的氢键而增溶蛋白。其中尿素的增溶效果稍差,异氰盐酸胍最强;去污剂,如SDS[7],可以破坏蛋白内的疏水键,可以增溶几乎所有的蛋白,但由于无法彻底去除而不允许用在制药行业中;酸,如70%甲酸[9],可以破坏蛋白
杆菌的包涵体可采用离心收获。 洗涤 包涵体常用的洗涤试剂为中性去垢剂和还原剂。包涵体中主要由重组蛋白组成,同时也含有一些外膜蛋白(Omp C、Omp F、Omp A)、16S 和 23S、5S的r RNA、质粒 DNA 和其它杂质。去除这些杂质,可采用去垢剂 Triton X-100、脱氧胆酸盐和低浓度的变性剂等对包涵体充分洗涤。包涵体洗涤的洁净程度,对于后续的纯化步骤十分重要,包涵体纯度高,可以大大降低后续的纯化压力。但是,变性剂尿素的使用应该注意的是大肠杆菌外膜蛋白Omp T(37 kD
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