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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:
6个月
- 英文名:
Recombinant Apolipoprotein O (APOO)
- 库存:
10000
- 供应商:
钰博生物
适用生物 Homo sapiens (Human,人)
载脂蛋白O(APOO)重组蛋白
产品应用 SDS-PAGE; WB; ELISA; IP. 规格 50ug
分子量 23.3kDa 价格 请咨询当地代理商
纯度 > 95%
来源 原核表达
| Organism species | Homo sapiens (Human) |
| Product No. | RPD742Hu01 |
| Source | Prokaryotic expression |
| Host | E.coli |
| Purity | > 95% |
| UOM | 50ug |
| Predicted Molecular Mass | 23.3kDa |
| Applications | SDS-PAGE; WB; ELISA; IP. |
| Endotoxin Level | <1.0EU per 1µg (determined by the LAL method) |
| Residues | Lys26~Lys198 with two N-terminal Tags, His-tag and T7-tag |
| Formulation | Supplied as lyophilized form in PBS, pH7.4, containing 5% trehalose, 0.01% sarcosyl. |
KDSP PKNSVKVDEL SLYSVPEGQS KYVEEARSQL EESISQLRHY CEPYTTWCQE TYSQTKPKMQ SLVQWGLDSY DYLQNAPPGF FPRLGVIGFA GLIGLLLARG SKIKKLVYPP GFMGLAASLY YPQQAIVFAQ VSGERLYDWG LRGYIVIEDL WKENFQKPGN VKNSPGTK
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.
载脂蛋白O(APOO)重组蛋白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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文献和实验在室温下配制: 10 × IB Solubilization buffer 5 mL ddH2 O 44.5 mL 30% N-lauroylsarcosine 0.5 mL DTT 50 µL
the reconstituted vial to sit at 4oC for at > 2 hours before use. (将重悬液在4oC静置2小时以上) 3. This solution can be stored at 2-8oC for up to 1 week. 第 3 步:该重悬液在 2-8oC 最长可保存 1 周。 用说明书上推荐的溶液将细胞因子或重组蛋白重悬到推荐的浓度后,细胞因子或重组蛋白可放置在2-8o C,即冰箱的冷藏室。在这种条件下,细胞因子或重组蛋白的活性
重组蛋白质的表达、纯化、复性和定量 按Qiagen公司的操作手册进行,具体步骤如下。 一、重组蛋白质的诱导表达 1.挑取转化有质粒的单菌落,接种于3ml 选择性LB液体培养基中,37 o C,250 rpm/min振摇培养过夜。 2.次日将培养过夜的菌液500 μl再接种于10 ml(1: 20)选择性LB液体培养基中,37 o C,250 rpm/min振摇培养至光密度(OD600 =0.6)时,取1 ml样本作为诱导前标本
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