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- 文献和实验
- 技术资料
- 保存条件:
-20℃
- 保质期:
6个月
- 英文名:
Recombinant WNT1 Inducible Signaling Pathway Protein 2 (WISP2)
- 库存:
10000
- 供应商:
钰博生物
适用生物 Homo sapiens (Human,人)
WNT1诱导信号通道蛋白2(WISP2)重组蛋白
产品应用 SDS-PAGE; WB; ELISA; IP. 规格 50ug
分子量 24.3kDa 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. | RPG894Hu01 |
| Source | Prokaryotic expression |
| Host | E.coli |
| Purity | > 95% |
| UOM | 50ug |
| Predicted Molecular Mass | 24.3kDa |
| Predicted isoelectric point | n/a |
| Applications | SDS-PAGE; WB; ELISA; IP. |
| Endotoxin Level | <1.0EU per 1µg (determined by the LAL method) |
| Subcellular Location | n/a |
| Residues | Gln24~Phe250 (Accession # O76076) with N-terminal His-Tag |
| Formulation | Supplied as lyophilized form in PBS, pH7.4, containing 5% trehalose, 0.01% sarcosyl. |
MGHHHHHHSGSEF-QLCPTPC TCPWPPPRCP LGVPLVLDGC GCCRVCARRL GEPCDQLHVC DASQGLVCQP GAGPGGRGAL CLLAEDDSSC EVNGRLYREG ETFQPHCSIR CRCEDGGFTC VPLCSEDVRL PSWDCPHPRR VEVLGKCCPE WVCGQGGGLG TQPLPAQGPQ FSGLVSSLPP GVPCPEWSTA WGPCSTTCGL GMATRVSNQN RFCRLETQRR LCLSRPCPPS RGRSPQNSAF
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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文献和实验摘要 Groundbreaking work demonstrated that ectopic expression of four transcription factors, Oct4, Klf4, Sox2, and c-Myc, could reprogram murine somatic cells to induced pluripotent stem cells (iPSCs) (Takahashi and Yamanaka, 2006), and human
【转帖】教你一种简单、高效的提高重组蛋白质的诱导表达量的方法
相信如何提高目的重组蛋白的诱导表达量是很多同学在研究中都会遇到的问题。记得小编在读书的时候就经常在研究这个问题,泡了无数论坛,看了无数帖子,尝试过IPTG的诱导浓度、培养基成分、诱导温度、诱导时间,甚至让别的公司帮忙做密码子优化(将目的片段通过全基因合成的方式合成出来)。总的来说,提高IPTG浓度是可以提高目的蛋白的诱导表达量的,但一般也就用到1mM的浓度,再高对细胞有毒性; 培养基营养越丰富,表达量越高,所以如果追求表达量的话,就不要用LB培养基了,用自动诱导培养基吧; 诱导温度,温度越低
近年来,重组蛋白的应用有了显著增长,与此同时,用于重组蛋白表达和纯化的技术和产品也得以增长。自从亲和标签融合技术出现以来,多种多样的短肽或蛋白亲和标签极大地方便了外源表达重组蛋白的分离与蛋白质复合体的纯化,已成为蛋白质研究领域不可或缺的工具。多聚组氨酸标签(His-tag)是目前高通量蛋白纯化最普遍使用的亲和标签,His 标签融合蛋白的固定化金属离子亲和层析(immobilized metal-ion affinity chromatography, IMAC)被作为主要的蛋白纯化方法。从重组蛋白
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