相关产品推荐更多 >

MRGPRD/MRGPRD蛋白Recombinant Human Mas-related G-protein coupled receptor member D (MRGPRD)重组蛋白Beta-alanine receptor;G-protein coupled receptor TGR7蛋白
¥9720
Z/Z蛋白/Zinc-binding protein蛋白/Recombinant Lassa virus RING finger protein Z (Z)重组蛋白
¥69
Recombinant-Escherichia-coli-Phosphoethanolamine-transferase-eptBeptBPhosphoethanolamine transferase eptB EC= 2.7.-.-
¥13790
Smpdl3b/Smpdl3b蛋白Recombinant Mouse Acid sphingomyelinase-like phosphodiesterase 3b (Smpdl3b)重组蛋白/蛋白
¥2328
Recombinant-Human-Olfactory-receptor-13C9OR13C9Olfactory receptor 13C9 Alternative name(s): Olfactory receptor OR9-13
¥11606
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
- 保质期:
Generally, the shelf life of liquid form is 6 months at -20℃/-80℃. The shelf life of lyophilized form is 12 months at -20℃/-80℃.
- 英文名:
Recombinant Human Threonine--tRNA ligase, mitochondrial (TARS2), partial
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 规格:
1mg/100μg/20μg
| 规格: | 1mg | 产品价格: | ¥10872.0 |
|---|---|---|---|
| 规格: | 100μg | 产品价格: | ¥2514.0 |
| 规格: | 20μg | 产品价格: | ¥1344.0 |
纯度:
Greater than 90% as determined by SDS-PAGE.基因名:
TARS2Uniprot No.:
Q9BW92别名:
Threonyl-tRNA synthetase ;ThrRSThreonyl-tRNA synthetase-like 1种属:
Homo sapiens (Human)蛋白长度:
Partial来源:
E.coli分子量:
55.3 kDa表达区域:
369-718aa氨基酸序列:
EHYQEDMFAVQPPGSDRPPSSQSDDSTRHITDTLALKPMNCPAHCLMFAHRPRSWRELPLRLADFGALHRAEASGGLGGLTRLRCFQQDDAHIFCTTDQLEAEIQSCLDFLRSVYAVLGFSFRLALSTRPSGFLGDPCLWDQAEQVLKQALKEFGEPWDLNSGDGAFYGPKIDVHLHDALGRPHQCGTIQLDFQLPLRFDLQYKGQAGALERPVLIHRAVLGSVERLLGVLAESCGGKWPLWLSPFQVVVIPVGSEQEEYAKEAQQSLRAAGLVSDLDADSGLTLSRRIRRAQLAHYNFQFVVGQKEQSKRTVNIRTRDNRRLGEWDLPEAVQRLVELQNTRVPNAEEIF蛋白标签:
N-terminal 6xHis-SUMO-tagged产品提供形式:
Liquid or Lyophilized powder缓冲液:
If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, pH 8.0.货期:
13-23 business days注意事项:
Repeated freezing and thawing is not recommended. Store working aliquots at 4℃ for up to one week.功能:
/内毒素:
Not test.SDS-PAGE:
(Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.LC-MS Image Description/Western Blot:
/Product types:
Developed ProteinBiological_Activity:
/Research Areas:
Epigenetics and Nuclear SignalingReconstitution:
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.Reference:
VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies.Diodato D., Melchionda L., Haack T.B., Dallabona C., Baruffini E., Donnini C., Granata T., Ragona F., Balestri P., Margollicci M., Lamantea E., Nasca A., Powell C.A., Minczuk M., Strom T.M., Meitinger T., Prokisch H., Lamperti C., Zeviani M., Ghezzi D.Hum. Mutat. 35:983-989(2014)Function:
Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Methods for Analysis of Mitochondrial tRNA Editing in Acanthamoeba castellanii
at the 5′ end of a tRNA substrate. The assay procedure involves RNA ligase-mediated joining of the 5′ and 3′ ends of a tRNA, use of the resulting circularized tRNA as template for cDNA synthesis primed by tRNA-specific primers over a region that encompasses
The Analysis of tRNA Import Into Mammalian Mitochondria
of corresponding genes from another organism (yeast) in the nucleus. We describe how to establish and to analyze such import mechanisms in cultured human cells. In detail, we describe (1) the construction of plasmids expressing importable yeast tRNA derivatives
Analysis of Mitochondrial DNA Mutations: Point Mutations
Since the first demonstration that mutations of the mitochondrial genome were associated with human disease, more than 100 pathological mitochondrial DNA (mtDNA) defects have been characterized in patients with a broad spectrum of clinical
技术资料暂无技术资料 索取技术资料





