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Xcessbio/Neural-LSB-Xcessbio Biosciences Inc/1000X; 0.5 ml/S10001

价格
¥1580.00
货号:S10001
浏览量:74
品牌:Xcess
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Product Information
Purity:≥98% for each compound
Storage:4oC for 3 month.-20oC for 6 month.
Cocktail Formulation:0.1 mM LDN-193189 and 10 mM SB431542 in DMSO solution

Biological Activity:

Differentiation of human pluripotent stem cells (hPSCs) requires precise signaling control at each step to mimic the embryonic development. Advances in using highly specific and potent small molecule modulators of signaling pathways have allowed efficient generation of nearly homogenous populations of specific cell types from hPSCs. For highly efficient conversion of hESCs/iPSCs into neural precursor cells in a monolayer fashion, inhibition of both BMP and TGFβ signaling pathways (i.e., dual SMAD inhibition) by small molecule inhibitors, LDN-193189 (0.1 µM) and SB431542 (10 µM) respectively (i.e., Neural-LSB), was developed as the most effective condition. Under this dual SMAD inhibition using the Neural-LSB small molecule cocktail, more than 80% of hPSCs are rapidly induced into Pax6+ neural precursor cells. This condition can be further combined with other patterning cues to generate subtype specific neural and neuronal cells, such as floor plate and midbrain dopaminergic neurons using Hedgehog and Wnt pathway activators (i.e., purmorphamine and CHIR99021), or nociceptors using 3i (combination of CHIR99021/GSK3 inhibitor, SU5402/FGF-VEGF-PDGF inhibitor, DAPT/Notch inhibitor).

XcessBio’s Neural-LSB contains the combination of LDN193189/BMP inhibitor and SB431542/TGFβ inhibitor.

How to Use:

  • In vitro: Simply add/dilute the received LSB stock solutions at 1:1000 into your hESC/iPSC differentiation basal media to make the LSB induction media and use it to initiate neural differentiation.

Reference:

  • 1. Chambers, S.M. et al. Combined small-molecule inhibition accelerates developmental timing and converts human pluripotent stem cells into nociceptors. (2012) Nature Biotechnology 30, 715-720.

  • 2. Chambers, S.M. et al. Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling. (2009) Nat. Biotechnol. 27, 275–280.

  • 3. Yu, P.B. et al. BMP type I receptor inhibition reduces heterotopic [corrected] ossification. (2008) Nat. Med. 14, 1363–1369.
  • Product Specification:
  • Kit-Neural-LSB_spec.pdf
  • Product MSDS:
  • Kit-neural-LSB_MSDS.pdf

Products are for research use only. Not for human use.

Xcess新型高效神经保护分子P7C32014年10月13日03:55  | 新闻印刷版刚刚在上个月的Cell中发表,最近关于神经保护小分子P7C3的 MOA研究具有广泛的体外和体内活性,为研究共享其他常见组织的神经系统疾病,损伤,发育和退行性疾病提供了新的令人兴奋的机会机制。  P7C3 是直接从体内神经发生筛选中鉴定出的无毒,稳定且可口服生物利用的合成小分子。它可以保护齿状回中的新生神经元,并刺激新神经元的生长。它还可以增强老年大鼠的学习和记忆能力。在爆炸介导的创伤性脑损伤(TBI)的啮齿动物模型中,P7C3还可以在损伤后,在神经元细胞死亡发生之前保持轴突的完整性。MOA研究表明P7C3可以结合烟酰胺磷酸核糖基转移酶(NAMPT),这是一种将烟酰胺转化为烟酰胺腺嘌呤二核苷酸(NAD)的限速酶。将活性P7C3化学物质施用至用阿霉素处理的细胞(诱导NAD耗竭),可导致细胞内NAD水平反弹,并免受阿霉素介导的毒性的影响。  如何订购:  Xcess Biosciences是一家领先的试剂和服务公司,提供10 mM DMSO溶液和以克计的固体形式的化合物。请访问我们的网站以获取订单信息和其他创新产品。特别是Xcess Biosciences继续向我们的表观遗传调节剂工具箱  (现在我们提供72种独特的化合物)和  泛素调节剂工具箱  (现在我们提供15种独特的化合物)中添加了更多新颖的小分子化学探针  。