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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
低温运输,4℃保存
- 保质期:
一年
- 英文名:
Transferrin Human(Partially Saturated)
- 库存:
大量
- 供应商:
上海钰博生物科技有限公司
- 规格:
10 mg/盒
别名: 铁传递蛋白; S i d e r o p h i l i n 。分子量: 7 5 0 0 0 ~ 8 0 0 0 0 ( 血清) ;76000~77000(伴清蛋白)。应用:生化研究。转铁蛋白是一种能传递铁离子的蛋白质,在大多数脊椎动物的血清中(血清铁传递蛋白)、蛋白中(伴清蛋白铁传递蛋白)和哺乳动物奶中(乳传递蛋白)发现的非血红素、铁结合的糖蛋白。
外观:粉红色冻干粉
纯度:≥98%
铁含量:300-600 μg/g
杂质:<1 EU/mg 内毒素
溶解性:溶于水,参考浓度2mg/mL。水溶液在4℃可保5-10天,过滤除菌后可增加其稳定性
L-转铁蛋白-Transferrin Human(Partially Saturated)低温运输,4℃保存,有效期一年。D3476-02 Yeast Plasmid Kit (200)-Q Spin Column
Omega快速过滤质粒抽提试剂盒系列
质粒快速中/大量提取试剂盒:快速从菌液中纯化250ug/1.0mg的高纯度质粒DNA
D6905-01 Fastfilter Plasmid Midi Kit(5)
D6905-03 Fastfilter Plasmid Midi Kit(25)
D6905-04 Fastfilter Plasmid Midi Kit(100)
D6924-01 Fastfilter Plasmid Maxi Kit(5)
D6924-03 Fastfilter Plasmid Maxi Kit(25)
D6924-04 Fastfilter Plasmid Maxi Kit(100)
96孔板快速过滤质粒提取试剂盒:以快速过滤板与结合配合操作提取质粒DNA
D1097-01 E-Z 96 Fastfilter Plasmid Kit(4x96)
D1097-02 E-Z 96 Fastfilter Plasmid Kit(20x96)
96孔板简单经济型质粒提取试剂盒:以一块过滤板式提取质粒DNA
D1095-01 E-Z 96 SE Plasmid Kit(4x96)
D1095-02 E-Z 96 SE Plasmid Kit(20x96)
Omega快速 无内毒素质粒抽提试剂盒系列
无内毒素小量质粒提取试剂盒 I/II:从培养过夜的菌液中提取30ug/70ug无内毒素质粒DNA
D6948-00 Endo-free Plasmid Mini Kit I(5)
D6948-01 Endo-free Plasmid Mini Kit I(50)
D6948-01* Endo-free Plasmid Mini Kit I(100)
D6948-02 Endo-free Plasmid Mini Kit I(200)
D6950-00 Endo-free Plamid Mini Kit II (5)
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文献和实验Deglycosylation of Glycoproteins Using Endoglycosidases
and must be determined empirically (Methods in Enzymology, 1994, 230 : 44-57). Human transferrin is an example of a glycoprotein containing two asparagine-linked -fucosyl-biantennary chains, one of which is only released slowly by endoglycosidases
Deglycosylation of Glycoproteins Using Endoglycosidases
and must be determined empirically (Methods in Enzymology, 1994, 230 : 44-57). Human transferrin is an example of a glycoprotein containing two asparagine-linked -fucosyl-biantennary chains, one of which is only released slowly by endoglycosidases
In Situ PCR Detection of HIV Expression in the Human Placenta
Control of vertical transmission of HIV-1 has progressed remarkably despite a lack of understanding of precise mechanisms by which infection may occur (1 ). The latter situation partially resulted from inadequate tools for in vitro analysis
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