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          目錄:愛(ài)必信(上海)生物科技有限公司>>細(xì)胞生物學(xué)>>重組蛋白>> abs04035CD105 (N-Trx, 6His)

          CD105 (N-Trx, 6His)
          • CD105 (N-Trx, 6His)
          參考價(jià) 840
          訂貨量 ≥1
          具體成交價(jià)以合同協(xié)議為準(zhǔn)
          840
          ≥1
          具體成交價(jià)以合同協(xié)議為準(zhǔn)
          • 品牌 absin
          • 型號(hào) abs04035
          • 廠商性質(zhì) 生產(chǎn)商
          • 所在地 上海市
          屬性

          供貨周期:一周 規(guī)格:10ug

          >

          更新時(shí)間:2024-07-08 15:24:14瀏覽次數(shù):862評(píng)價(jià)

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          供貨周期 一周 規(guī)格 10ug
          愛(ài)必信特色產(chǎn)品線(全部現(xiàn)貨):
          二抗、標(biāo)簽抗體、對(duì)照抗體;WB相關(guān):ECL發(fā)光液、預(yù)染marker、預(yù)制膠;IHC相關(guān):二抗試劑盒、組化筆;IP/CoIP試劑盒;細(xì)胞因子、信號(hào)通路調(diào)節(jié)劑;血清、BSA、蛋白酶K、CTB、TTX、CEE;凋亡試劑盒、呼吸爆發(fā)試劑盒;動(dòng)植物提取物...
          概述
          描述Recombinant Human Endoglin is produced by our E.coli expression system and the target gene encoding Glu26-Gln176 is expressed with a Trx, 6His tag at the N-terminus.
          別名Endoglin, END, CD105, ENG
          形態(tài)Supplied as a 0.2 μm filtered solution of 20mM PB,150mM NaCl,pH7.4.
          來(lái)源E. coli
          氨基酸序列MSDKIIHLTDDSFDTDVLKADGAILVDFWAEWCGPCKMIAPILDEIADEYQGKLTVAKLNIDQNP GTAPKYGIRGIPTLLLFKNGEVAATKVGALSKGQLKEFLDANLAGSGSGHMHHHHHHSSGLVPRG SGMKETAAAKFERQHMDSPDLGTDDDDKAMETVHCDLQPVGPERDEVTYTTSQVSKGCVAQAPNA ILEVHVLFLEFPTGPSQLELTLQASKQNGTWPREVLLVLSVNSSVFLHLQALGIPLHLAYNSSLV TFQEPPGVNTPSFPKTQILEWAAERGPITSAAELNDPQSILLRLGQAQ
          內(nèi)毒素水平Less than 0.1 ng/μg (1 IEU/μg) as determined by LAL test.
          Accession #P17813
          性能
          背景Endoglin is a single-pass type I membrane protein which restricted to endothelial cells in all tissues except bone marrow. Endoglin as major glycoprotein of vascular endothelium, it has been found on endothelial cells, activated macrophages, fibroblasts, and smooth muscle cells. Furthermore, Homodimer forms a heteromeric complex with the signaling receptors for transforming growth factor-beta: TGFBR1 and/or TGFBR2. It may have an important role in the binding of endothelial cells to integrins and/or other RGD receptors. Defects in ENG are the cause of hereditary hemorrhagic angiectasia type 1 (HHT1), which is an autosomal dominant multisystemic vascular dysplasia, characterized by recurrent epistaxis, muco-cutaneous angiectases, gastro-intestinal hemorrhage, and pulmonary (PAVM), cerebral (CAVM) and hepatic arteriovenous malformations.
          保存方法Store at < -20°C, stable for 6 months after receipt. Please minimize freeze-thaw cycles.
          純度Greater than 95% as determined by reducing SDS-PAGE

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