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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Purified recombinant sugarcane SPS1 protein (C-terminal 362 amino acids with His6 Tag at the N-terminus)
- 亚型:
IgG
- 形态:
Liquid
- 保存条件:
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性:
Polyclonal
- 标记物:
Unconjugated
- 适应物种:
Zea mays, Sugarcane
- 保质期:
12 months from the shipping date of the product.
- 抗原来源:
Sugarcane
- 目录编号:
GTX00931
- 级别:
Primary Antibodies
- 库存:
Available
- 供应商:
GeneTex
- 宿主:
Rabbit
- 应用范围:
WB, ELISA
- 浓度:
4 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点:
Sucrose-Phosphate Synthase
- 抗体英文名:
Sucrose-Phosphate Synthase antibody
- 抗体名:
Sucrose-Phosphate Synthase 抗体
- 规格:
200 μg
WB analysis of E. coli transformed with SPS 1 overexpressing plasmid: pTrcSPS (full length of SPS) or pTrcHisSPS (full length with His6 Tag) and were harvested at the indicated time points after IPTG induction using GTX00931 Sucrose-Phosphate Synthase antibody. The lower band is a truncated SPS protein. Molecular size markers in the 2nd lane are 150, 100 and 75 kDa.
WB analysis of maize leaf extract using GTX00931 Sucrose-Phosphate Synthase antibody.
Dilution : 1:500
Loading : 20 μg
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文献和实验Application of Sucrose Synthase in the Synthesis of Nucleotide Sugars and Saccharides
The realization that the oligosaccharide moieties of glycoconjugates, such as glycoproteins and glycolipids, are involved in important intra- and intercellular of important oligosaccharide structures as tools in analytical and therapeutic
氨甲酰磷酸合酶 carbamoyl phosphate synthase
催化由 NH3 、 CO2 与 2分子的 ATP合成氨甲酰磷酸的不可逆反应的酶, EC2. 7. 2. 5。存在于哺乳类的肝脏、蛙的肝脏、大肠杆菌等,分子量 31.5万(蛙肝)。对于动物酶的活性, N-乙酰谷氨酸是必需的,经此酶生成的氨甲酰磷酸是生成精氨酸、尿素或合成嘧啶的素材。大肠杆菌的酶亦能利用谷酰胺作为氨基供体。此外在蕈类,如伞菌( Agaricus),存在着只利用谷酰胺作为氨基供体的酶( EC2. 7. 2. 9)。
which distinguishes the biosynthetic pathways of H4MPT and tetrahydrofolate is ribofuranosylaminobenzene 5′-phosphate synthase (RFAP synthase). Given the importance of RFAP synthase in H4 MPT biosynthesis, the identification of putative RFAP synthase genes
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