Comparativeassessmentofglycosylationofrecombinanthuman...（五）
Supporting Information(1) RP-UPLC-Q-TOF analysis of hFSHs subunits; (2) molecular weights and possible glycan structures of hFSHs subunits; (3) profiling and relative quantification of N-glycans of hFSHs; (4) site-specific characterization of N-glycosylation of rhFSH and uhFSH. AcknowledgmentsThis work was supported by Shanghai Sailing Program (15YF1410900), Shanghai Technology Standard Program (14DZ050210......阅读全文
Comparative－assessment－of－glycosylation－of－recombinant－human－...（五）
Supporting Information(1) RP-UPLC-Q-TOF analysis of hFSHs subunits; (2) molecular weights and possible glycan structures of hFSHs subunits; (3) pr
Comparative－assessment－of－glycosylation－of－recombinant－human－...（四）
Site-specific characterization of N-glycansFor intact N-glycopeptide analysis, chymotryptic digests of both hFSHs were subjected under UPLC equipped
Comparative－assessment－of－glycosylation－of－recombinant－human－...（一）
Comparative assessment of glycosylation of recombinant human FSH and highly purified FSHHong Wang, Xi Chen, Xiaoxi Zhang, Wei Zhang, Yan Li, Hongrui Y
Comparative－assessment－of－glycosylation－of－recombinant－human－...（六）
(22) Wu, S. W.; Pu, T. H.; Viner, R.; Khoo, K. H. Novel LC-MS/MS product dependent parallel data acquisition function and data analysis workflow f
Comparative－assessment－of－glycosylation－of－recombinant－human－...（七）
Figure 3 MS2 spectra of 2-AB-labeled N-glycan structures. Diagnostic ions are marked with corresponding fragment structures. (a) NeuGc1NeuAc1HexNA
Comparative－assessment－of－glycosylation－of－recombinant－human－...（二）
Experimental sectionChemicals and reagentsOne lot of PuregonR-HP of 50 IU/0.5mL and two lots of PuregonR-HP of 100 IU/0.5mL (rhFSH) (Organon, Oss, N
Comparative－assessment－of－glycosylation－of－recombinant－human－...（三）
LC-MS data processingN-glycan data were processed using UNIFI 1.7 with Glycobase 3+ (Waters Corporation, Milford, MA) for N-glycan structure. The pe
Synthesis－of－Recombinant－Human－Cytokine－GMCSF－in－the－－Seeds－of－Transge...
We are interested in studying plant systems as vehicles for the production of recombinant proteins of clinical relevance. There are a number of po
重组人表皮细胞生长因子（recombinant－human－EGF）
生物学功能：人表皮细胞生长因子（hEGF）不仅对上皮细胞而且对许多类型细胞均有促增殖作用，是与细胞的生长及分化有关的重要生长因子。hEGF具有多种生物活性，主要表现在：①在体内刺激皮肤组织、角膜和气管上皮组织的生长繁殖； ②加速角膜、皮肤等表皮创伤的修复； ③抑制胃酸分泌；④促进人皮肤上皮细胞、角膜
Comprehensive－identification－of－novel－proteins－and－Nglycosylation－sites五
RJ provides efficient energetic fuels for the fast development of larvae and the egg-laying queen through the metabolism of sugars, lipids, and pr
流式应用精选——微核检测（体内体外）
注：点击文章名称查看详情。文章名称样本仪器型号备注Assessment of the Genotoxic Potential of Azidothymidine in the Comet,Micronucleus, and Pig-a AssayBone Marrow and Peripheral
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CO2恒温摇床解决人胚肾－293－(HEK293)－细胞结团问题（一）
人胚肾 293 (HEK293) 细胞在重组蛋白表达中是最常见的宿主细胞。 这类细胞能够表达大量的膜蛋白，如 G 蛋白偶联受体 (GPCR) ，是无法在最常见的生物制药生产宿主，如：中国仓鼠卵巢 (CHO) 细胞中作表达。 HEK293 虽然是蛋白表达的极好宿主，然而 HEK293 细胞
In－vitro－Assessment－of－Metabolic－－in－Suspension－Cryopreserved－Hepatocytes
实验概要BackgroundThe pharmaceutical and biotechnology industry’s goal is to discover therapeutic agents that are both safe and effective at treating or
Glycosylation－of－Antibody－Therapeutics:－Optimisation－for－Purpose
Recombinant antibody therapeutics represent a significant success story in terms of clinical benefit delivered and revenue (profit) generated with
Comprehensive－identification－of－novel－proteins－and－Nglycosylation－sites九
41. Schmidt O, Theopold U, Strand M: Innate immunity and its evasion and suppression by hymenopteran endoparasitoids. BioEssays 2001, 23(4):344–35
Assessment－of－Magnaporthe－grisea－mating－type－by－spore－PCR
Isolation of DNA from filamentous fungi for PCR analysis is usually time consuming and involves use of toxic chemicals such as phenol/chloroform. In S
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Plants have emerged in the past decade as a suitable alternative to the current production systems for recombinant pharmaceutical proteins and, toda
欧盟评估一种转基因大豆作为食品和饲料的安全性
2019年11月11日，欧盟食品安全局（EFSA）发布消息，欧盟食品安全局转基因生物小组（GMO Panel）评估了转基因大豆MON 87751×MON 87701×MON 87708×MON 89788用作食品和饲料的安全性。 经过评估，GMO小组得出结论，就对人类和动物健康以及环境的潜在影
Preparation－of－human－platelets
Preparation of human platelets 1. Human blood was taken from drug-free volunteers on the day of the experiment using acidic citrate dextrose
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Remove Human ES cells from liquid nitrogen storage tank. Fill out a freeze/thaw form.Thaw cryovial by gently swirling in waterbath until only a small
Human－Embryonic－Stem－(ES)－Cell－Protocols——Freezing－Human－ES－Cells
Collagenase cells for approximately 7 minutes at 37 °C (until edges of colonies are curling up).With a 5 ml pipet, gently pipet and scrape colonies f
Steps－in－the－Glycosylation－of－Mammalian－Nlinked－Oligosaccarides
The biosynthesis pathway of N-glycans is a costly system with respect to the number of enzymes that are involved in the synthesis and trimming of N-gl
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Expression of foreign proteins in plants has become a standard technique in plant molecular biology. Various plant species have been used to produ
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Induction of BRF in bacteria and purification on Ni-NTA agaroseTransform BRF plasmid into strain BL21 DE3 (pLysS) or JM25 (DE3 containing the Arg tRNA
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Human－Embryonic－Stem－(ES)－Cell－Protocols——Splitting－Human－ES－cells－on－MEFs
based on splitting onto one plateWarm collagenase IV split media to 37 °C in a water bath.Aspirate media off of cell culture plate.Add the following a
Human－Embryonic－Stem－(ES)－Cell－Protocols—Splitting－Human－ES－cells－onMatrige
based on splitting onto on plateWarm collagenase media to 37°C in a water bath.Aspirate media off of cell culture plate.Add the following amount of co
典型CASE分享－蛋白产品常见翻译后修饰（PTM）
翻译后修饰（PTM）是指蛋白质在翻译后发生的化学修饰。抗体在生产、贮存及临床使用过程中，均可能产生各类翻译后修饰变异体。翻译后修饰可能导致抗体所带的电荷乃至结构发生变化，从而影响其与抗原及Fc受体的亲和力，进而影响抗体药物的活性等关键质量属性。因此，对抗体药物的各类翻译后修饰进行表征和工艺控制是有必
使用CO2恒温摇床解决人胚肾－293－(HEK293)－细胞结团问题
人胚肾 293 (HEK293) 细胞在重组蛋白表达中是最常见的宿主细胞。 这类细胞能够表达大量的膜蛋白，如 G 蛋白偶联受体 (GPCR) ，是无法在最常见的生物制药生产宿主，如：中国仓鼠卵巢 (CHO) 细胞中作表达。 HEK293 虽然是蛋白表达的极好宿主，然而 HEK293 细胞