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当前位置: 首页 > 产品中心 > Primary_cell > Iwai Chem/iMatrix-511(尺寸175ug-样品尺寸)***仅限一次性购买***/细胞培养/N-892013
商品详细Iwai Chem/iMatrix-511(尺寸175ug-样品尺寸)***仅限一次性购买***/细胞培养/N-892013
Iwai Chem/iMatrix-511(尺寸175ug-样品尺寸)***仅限一次性购买***/细胞培养/N-892013
Iwai Chem/iMatrix-511(尺寸175ug-样品尺寸)***仅限一次性购买***/细胞培养/N-892013
商品编号: N-892013
品牌: Iwai
市场价: ¥0.00
美元价: 0.00
产地: 美国(厂家直采)
公司:
产品分类: 原代细胞
公司分类: Primary_cell
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Product Description

iMatrix-511 Product SummaryLaminin 511 is known to bind to Intergin α6β1 of the cell surface. iMatrix-511 is highly purified human Laminin 511-E8 fragments recombinantly expressed by CHO-S cell.ApplicationiMatrix-511 can be used as cell culture matrix for various cell types including ES/iPS cells.ContentsLiquid Solution (175μg/vial @ 0.5 mg/mL Solvent: PBS(-)) .Product Size: 350μg (175μg x 2 pcs.)SpecificationsFormat: Solution (175μg/vial @ 0.5 mg/mL)Storage temperature: 2-15°CNaCl concentration: 137 mMActivityThe dissociation constant of the binding activity with integrin α6β1 is under 10 nM.

Procedure1. Dilute the solution with PBS (-). Coat dishes with 0.5μg/cm². The optimal coating concentration depends on cell lines from 0.1 to 1.5μg/cm². (For example, when you use 6-well plate (9.6 cm²/well), add 9.6μl iMatrix-511 (4.8ug) in 1.99ml of PBS(-). Add 2 mL of diluted iMatrix-511 solution to the well.)2. Incubate for 1 hour at 37°C, 3 hours at Room temperature, or over night at 4°C.3. Remove excess fluid from the coated surface. No rinse is needed.4. Immediately plate the cells at desired density.Notes:Don"t allow the plate to dry. Briefly spin down all liquid in the tube before use. Avoid repeated freeze-thaw cycles.DocumentationDownload Protocol [PDF]Download MSDS [PDF]Product Basics & StructureiMatrix-511 is an innovative cell culture matrix compatible with a wide variety of cell types, and exceptionally well suited for pluripotent stem cells. This product is comprised of recombinant Laminin-511 E8 protein fragments which permit ES/iPS cells to be maintained in xeno-free culture conditions, enable the passaging of single cells, and provide greater adhesion than full-length Laminin, Vitronectin or Matrigel⁵.Laminin-511 is a major component of the basement membrane used as a scaffold for pluripotent stem cells (ES/iPS cells), as it binds to integrin on cell surfaces. However Laminin-511 is a large protein (800kDa) composed of three chains (α-, β-, and γ-) forming a supramolecular aggregate, making it difficult to produce recombinantly. In order to overcome this challenge, Laminin-511 proteins were fragmented to find the smallest integrin-binding component and the E8 fragment was identified as the most promising result. In fact, hES cells were found to adhere more strongly to the E8 fragment than to the full-length protein.

In the study referenced above, the Laminin-511 E8 fragment and other cell culture substrates were compared for their strength in adhering to hES cells. The horizontal axis of the graph shows the concentration of cell culture substrate, and the vertical axis, the OD value (optical density at 570nm). This result shows that the Laminin-511 E8 fragment adheres to cells more strongly than its competitors.

In the same study cited above, Human ES cells were passaged on Laminin-511 E8 fragment and other cell culture substrates. Upon singly dispersing human ES cell colonies at the time of passage, it was confirmed that single cells adhere rapidly to Laminin-511 E8 and proliferate immediately.

Reference Literature

1. Miner, JH and Yurchenco, PD Laminin functions in tissue morphogenesis. Annu. Rev. Cell Dev. Biol. 20, 255-284 (2004).https://doi.org/10.1146/annurev.cellbio.20.010403.0945552. Ido H, Harada K, Futaki S, Hayashi Y, Nishiuchi R, Natsuka Y, Li S, Wada Y, Combs AC, Ervasti JM and Sekiguchi K. Molecular dissection of the alpha-dystroglycan- and integrin-binding sites within the globular domain of human laminin-10. J. Biol. Chem. 279, 10946-10954 (2004).https://doi.org/10.1074/jbc.M3136262003. Ido H, Nakamura A, Kobayashi R, Ito S, Li S, Futaki S and Sekiguchi K. The requirement of the glutamic acid residue at the third position from the carboxyl termini of the laminin gamma chains in integrin binding by laminins. J. Biol. Chem. 282, 11144-11154 (2007).https://doi.org/10.1074/jbc.M6094022004. Taniguchi Y, Ido H, Sanzen N, Hayashi M, Sato-Nishiuchi R, Futaki S and Sekiguchi K. The C-terminal region of laminin beta chains modulates the integrin binding affinities of laminins. J. Biol. Chem. 284, 7820-7831 (2009).https://doi.org/10.1074/jbc.M8093322005. Miyazaki T, Futaki S, Suemori H, Taniguchi Y, Yamada M, Kawasaki M, Hayashi M, Kumagai H, Nakatsuji N, Sekiguchi K and Kawase E. Laminin E8 fragments support efficient adhesion and expansion of dissociated human pluripotent stem cells. Nat. Commun. 3, 1236 (2012).https://doi.org/10.1038/ncomms22316. Nakagawa M, Taniguchi Y, Senda S, Takizawa N, Ichisaka T, Asano K, Morizane A, Doi D, Takahashi J, Nishizawa M, Yoshida Y, Toyoda T, Osafune K, Sekiguchi K, Yamanaka S. A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells. SCIENTIFIC REPORTS | 4 : 3594 | doi:10.1038/srep035947. Yasuhiro Takashima, Ge Guo, Remco Loos, Jennifer Nichols, Gabriella Ficz, Felix Krueger, David Oxley, Fatima Santos, James Clarke, William Mansfield, Wolf Reik, Paul Bertone, Austin Smith Resetting Transcription Factor Control Circuitry toward Ground-State Pluripotency in Human. Cell Volume 158, Issue 6, p1254–1269, 11 September 2014 doi:10.1016/j.cell.2014.08.0298. Doi D et al. (2014). Isolation of Human Induced Pluripotent Stem Cell-Derived Dopaminergic Progenitors by Cell Sorting for Successful Transplantation.Stem Cell Reports. 2 (3): 337-50.https://doi.org/10.1016/j.stemcr.2014.01.0139. Takashima Y et al. (2014). Resetting Transcription Factor Control Circuitry toward Ground-State Pluripotency in Human. Cell. 158 (6): 1254-69.https://doi.org/10.1016/j.cell.2014.08.02910. Fukuta M et al. (2014). Derivation of mesenchymal stromal cells from pluripotent stem cells through a neural crest lineage using small molecule compounds with defined media.PLos One. 9 (12) : e112291.https://doi.org/10.1371/journal.pone.011229111. Hayashi et al. (April 2015). Structure-based discovery of NANOG variant with enhanced properties to promote self-renewal and reprogramming of pluripotent stem cells. PNAS vol. 112 (15): 4666-4671.https://doi.org/10.1073/pnas.1502855112

FOR RESEARCH USE ONLY, NOT FOR USE IN DIAGNOSTIC PROCEDURES.

Manufactured by: Nippi, Inc.*License to manufacture and sell this product has been obtained from Osaka University & Kyoto University.*

品牌介绍
Iwai-Chem岩井北美有限公司是岩井化学株式会社(位于日本)的美国全资子公司,成立于2006年,是岩井向国际市场扩张的一部分。致力于弥合美国和日本生命科学产业之间的鸿沟,北美洲岩井提供了从日本到美国市场的高质量试剂和研究工具,同时还向日本提供了美国技术和产品。    历史:* 1947年4月–岩井化学株式会社在日本东京成立 * 2006年10月–岩井北美有限公司在加利福尼亚州伯灵格姆成立。* 2007年9月–收购了Iwai USA Inc.及其所有资产,  包括Chondrex,Inc.的多数股权。 * 2009年2月–办公室迁至加利福尼亚福斯特城* 2017年4月-办公室搬迁至加利福尼亚州圣卡洛斯的当前地址 关于  岩井化学株式会社  (日本): 岩井化学株式会社成立于1947年,位于日本东京,旨在生产和分配高纯度试剂。在过去的七十年中,岩井化学一直秉持“诚信”作为其管理理念的基石,并深知只有赢得客户的信任,企业才能继续创新和发展。自岩井创立以来,生命科学研究领域取得了显着进展,特别是在分子生物学,基因工程和免疫学领域。通过对这些研究领域中对专用试剂的需求进行预测并采取行动,并与国内外主要制造商建立合作伙伴关系,从而形成了一条完整的产品线,岩井化学已达到了目前的行业领导者地位。如今,岩井化学公司拥有70多名销售人员,为450多家制药公司,大学和研究机构的2500多个研究实验室提供服务,年销售额约为1.6亿美元,这使岩井化学公司占据了日本全部生物制品的10%试剂零售市场。