1,3-b-D葡聚糖内切酶[木霉菌] endo-1,3-β-D-Glucanase (Trichoderma sp.) 货号:E-CELTH Megazyme中文站

1,3-b-D葡聚糖内切酶[木霉菌]

英文名:endo-1,3-β-D-Glucanase (Trichoderma sp.)

货号:E-CELTH

规格:

 High purity recombinant Cellulase (endo-1,4-β-D-glucanase) (Alkali Stable) (Thermobifida halotolerans) for use in research, biochemical enzyme assays andin vitro diagnostic analysis.

EC 3.2.1.4
CAZy Family: GH6
CAS: 9012-54-8

1,4-beta-D-glucan 4-glucanohydrolase

Recombinant. From Thermobifida halotolerans.
In 3.2 M ammonium sulphate.
Supplied at ~ 150 U/mL. 

Specific activity: ~ 27 U/mg protein (on CM-Cellulose 4M) at pH 8.5 and 60oC;
                           ~ 16 U/mg protein (on CM-Cellulose 4M) at pH 8.5 and 40oC. 

Stability: > 4 years at 4oC.

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合成·反应装置ケミスト广场CPG – 2000系列用SPC两口反应容器200毫升(CPG – 2120用)|柴田科技有限公司-环境检测设备、科学仪器的制造销售

产品详细

科学仪器

合成·反应装置ケミスト广场CPG – 2000系列用SPC两口反应容器200毫升(CPG – 2120用)

合成·反应装置ケミスト广场CPG - 2000系列用SPC两口反应容器200毫升(CPG - 2120用)|柴田科技有限公司-环境检测设备、科学仪器的制造销售

  • 合成·反应装置ケミスト广场CPG - 2000系列用SPC两口反应容器200毫升(CPG - 2120用)|柴田科技有限公司-环境检测设备、科学仪器的制造销售

商品代码其他情报(式样)

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产品照片 合成·反应装置ケミスト广场CPG - 2000系列用SPC两口反应容器200毫升(CPG - 2120用)|柴田科技有限公司-环境检测设备、科学仪器的制造销售
商品代码 054310 – 2612
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价格(不含税) 18万日元。

上海金畔生物科技有限公司

663%2F%3Fc%3D34& ” 663%2F%3Fc%3D34&

Phos-tag™ 琼脂糖吸管


产品编号 产品名称 产品规格 产品等级 产品价格
387-07321 Phos-tag™ Tip 
Phos-tag™ 琼脂糖吸管
8个

Phos-tag™ 琼脂糖吸管Phos-tag™ 琼脂糖吸管

Phos-tag™ Tip

  可特异性捕捉磷酸基团的功能性分子“Phos-tag ™”的磷酸化肽纯化用枪头。

  枪头里含有Phos-tag ™ 琼脂糖,是即开即用的前处理工具,适用于生理状态下低分子量磷酸化分子(核酸和多肽等)的分离和富集。


原理


把Phos-tagTM Tip 装在注射器(购买产品附送)上使用。


                                   Phos-tag™ 琼脂糖吸管 

                                                           

Phos-tag ™ Tip 的结构


Phos-tag™ 琼脂糖吸管

优点、特色


 操作时间少于30分钟。       

 高回收率可重复利用。

 无需昂贵仪器。

 缓冲液为生理pH 条件下。


Phos-tag™ 琼脂糖吸管

案例、应用


分离磷酸化肽使用例


Phos-tag™ 琼脂糖吸管






Phos-tag™ 系列

磷酸化蛋白新方法!

  Phos-tag™是一种能与磷酸离子特异性结合的功能性分子。它可用于磷酸化蛋白的分离(Phos-tag™ Acrylamide)、Western Blot检测(Phos-tag™ Biotin)、蛋白纯化 (Phos-tag™Agarose)及质谱分析MALDI-TOF/MS (Phos-tag™ Mass Analytical Kit)。


◆Phos-tag™ 的基本结构

Phos-tag™ 琼脂糖吸管



原理:


Phos-tag™ 琼脂糖吸管



特点:


●   与-2价磷酸根离子的亲和性和选择性高于其它阴离子

●   在pH 5-8的生理环境下生成稳定的复合物

相关应用:


Phos-tag™ 琼脂糖吸管

相关产品:

 产品名称

 用  途

 Phos-tag™ Acrylamide

 分离: SDS – PAGE 分离不同磷酸化水平的蛋白

 SuperSep Phos-tag™

 分离: 预制胶中含有50μM Phos-tag™ Acrylamide

 Phos-tag™ Biotin

 检测: 代替 Western Blot 检测中的磷酸化抗体

 Phos-tag™ Agarose

 纯化: 通用柱层析,纯化磷酸化蛋白

 Phos-tag™ Mass

 Analytical Kit

 分析: 用于质谱 MALDI-TOF/MS 分析,提高磷酸化分子的检测灵敏度


phos-tag™由日本广岛大学研究生院医齿药学综合研究科医药分子功能科学研究室开发。

更多产品信息,请点击:http://phos-tag.jp

Phos-tag™ 琼脂糖吸管

Phos-tag 第5版说明书

Phos-tag™ 琼脂糖吸管

Phos-tag系列 ver 5

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·  Fine tuning chloroplast movements through physical interactions between phototropins[J]. Journal of Experimental Botany, 2016: erw265,Sztatelman O, Łabuz J, Hermanowicz P, et al.

·  Characterization of the Neospora caninum NcROP40 and NcROP2Fam-1 rhoptry proteins during the tachyzoite lytic cycle[J]. Parasitology, 2016, 143(01): 97-113,Pastor-Fernandez I, Regidor-Cerrillo J, Jimenez-Ruiz E, et al.

·  Transcriptional Profile during Deoxycholate-Induced Sporulation in a Clostridium perfringens Isolate Causing Foodborne Illness[J]. Applied and environmental microbiology, 2016, 82(10): 2929-2942,Yasugi M, Okuzaki D, Kuwana R, et al.

·  Timely Closure of the Prospore Membrane Requires SPS1 and SPO77 in Saccharomyces cerevisiae[J]. Genetics, 2016: genetics. 115.183939,Paulissen S M, Slubowski C J, Roesner J M, et al.

·  DDK dependent regulation of TOP2A at centromeres revealed by a chemical genetics approach[J]. Nucleic Acids Research, 2016: gkw626,Wu K Z L, Wang G N, Fitzgerald J, et al.

·  OVATE Family Protein 8 Positively Mediates Brassinosteroid Signaling through Interacting with the GSK3-like Kinase in Rice[J]. PLoS Genet, 2016, 12(6): e1006118,Yang C, Shen W, He Y, et al.

·  Epithelial Sel1L is required for the maintenance of intestinal homeostasis[J]. Molecular biology of the cell, 2016, 27(3): 483-490, Sun S, Lourie R, Cohen S B, et al.

·  Effect of Sodium Dodecyl Sulfate Concentration on Supramolecular Gel Electrophoresis[J]. ChemNanoMat, 2016,Tazawa S, Kobayashi K, Yamanaka M.

·  Intergenic VNTR Polymorphism Upstream of rocA Alters Toxin Production and Enhances Virulence in Streptococcus pyogenes[J]. Infection and immunity, 2016: IAI. 00258-16,Zhu L, Olsen R J, Horstmann N, et al.

·  Ajuba Phosphorylation by CDK1 Promotes Cell Proliferation and Tumorigenesis[J]. Journal of Biological Chemistry, 2016: jbc. M116. 722751,Chen X, Stauffer S, Chen Y, et al.

·  Editorial: International Plant Proteomics Organization (INPPO) World Congress 2014[J]. Frontiers in Plant Science, 2016, 7,Heazlewood J L, Jorrín-Novo J V, Agrawal G K, et al.

·  Phosphoinositide kinase signaling controls ER-PM cross-talk[J]. Molecular biology of the cell, 2016, 27(7): 1170-1180,Omnus D J, Manford A G, Bader J M, et al.

·  A multiple covalent crosslinked soft hydrogel for bioseparation[J]. Chemical Communications, 2016, 52(15): 3247-3250,Liu Z, Fan L, Xiao H, et al.

·  Advances in crop proteomics: PTMs of proteins under abiotic stress[J]. Proteomics, 2016, 16(5): 847-865,Wu X, Gong F, Cao D, et al.

·  Cyclin-Dependent Kinase Co-Ordinates Carbohydrate Metabolism and Cell Cycle in S. cerevisiae[J]. Molecular cell, 2016, 62(4): 546-557,Zhao G, Chen Y, Carey L, et al.

·  Carbon Monoxide Gas Is Not Inert, but Global, in Its Consequences for Bacterial Gene Expression, Iron Acquisition, and Antibiotic Resistance[J]. Antioxidants & redox signaling, 2016,Wareham L K, Begg R, Jesse H E, et al.

·  Two-layer regulation of PAQR3 on ATG14-linked class III PtdIns3K activation upon glucose starvation[J]. Autophagy, 2016: 1-2,Xu D, Wang Z, Chen Y.

·  Regulation of sphingolipid biosynthesis by the morphogenesis checkpoint kinase Swe1[J]. Journal of Biological Chemistry, 2016, 291(5): 2524-2534,Chauhan N, Han G, Somashekarappa N, et al.

·  PAX5 tyrosine phosphorylation by SYK co-operatively functions with its serine phosphorylation to cancel the PAX5-dependent repression of BLIMP1: A mechanism for antigen-triggered plasma cell differentiation[J]. Biochemical and biophysical research communications, 2016, 475(2): 176-181,Inagaki Y, Hayakawa F, Hirano D, et al.

·  A Combined Computational and Genetic Approach Uncovers Network Interactions of the Cyanobacterial Circadian Clock[J]. Journal of Bacteriology, 2016: JB. 00235-16,Boyd J S, Cheng R R, Paddock M L, et al.

·  HuR mediates motility of human bone marrow-derived mesenchymal stem cells triggered by sphingosine 1-phosphate in liver fibrosis[J]. Journal of Molecular Medicine, 2016: 1-14,Chang N, Ge J, Xiu L, et al.

·  Combined replacement effects of human modified β-hexosaminidase B and GM2 activator protein on GM2 gangliosidoses fibroblasts[J]. Biochemistry and Biophysics Reports, 2016,Kitakaze K, Tasaki C, Tajima Y, et al.

·  Roseotoxin B Improves Allergic Contact Dermatitis through a Unique Anti-inflammatory Mechanism Involving Excessive Activation of Autophagy in Activated T-Lymphocytes[J]. Journal of Investigative Dermatology, 2016,Wang X, Hu C, Wu X, et al.


References on Phos-tag™ Chemistry

  • Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry of phosphorylated compounds using a novel phosphate capture moleculeRapid Communications of Mass Spectrometry17, 2075-2081 (2003), H. Takeda, A. Kawasaki, M. Takahashi, A. Yamada, and T. Koike 

  • Recognition of phosphate monoester dianion by an alkoxide-bridged dinuclear zinc (II) complexDalton Transactions, 1189-1193 (2004), E. Kinoshita, M. Takahashi, H. Takeda, M. Shiro, and T. Koike

  • Quantitative analysis of lysophosphatidic acid by time-of-flight mass spectrometry using a phosphate capture molecule, Journal of Lipid Research45, 2145-2150 (2004), T. Tanaka, H. Tsutsui, K. Hirano, T. Koike, A. Tokumura, and K. Satouchi

  •  Production of 1,2-Didocosahexaenoyl Phosphatidylcholine by Bonito Muscle Lysophosphatidylcholine/TransacylaseJournal of Biochemistry,136, 477-483 (2004), K. Hirano, H. Matsui, T. Tanaka, F. Matsuura, K. Satouchi, and T. Koike

  • Novel immobilized zinc(II) affinity chromatography for phosphopeptides and phosphorylated proteins, Journal of Separation Science, 28, 155-162 (2005), E. Kinoshita, A. Yamada, H. Takeda, E. Kinoshita-Kikuta, and T. Koike

  • Detection and Quantification of On-Chip Phosphorylated Peptides by Surface Plasmon Resonance Imaging Techniques Using a Phosphate Capture MoleculeAnalytical Chemistry77, 3979-3985 (2005), K. Inamori, M. Kyo, Y. Nishiya, Y. Inoue, T. Sonoda, E. Kinoshita, T. Koike, and Y. Katayama

  • Phosphate-binding tag: A new tool to visualize phosphorylated proteins, Molecular & Cellular Proteomics, 5, 749-757 (2006), E. Kinoshita, E. Kinoshita-Kikuta, K. Takiyama, and T. Koike

  • Enrichment of phosphorylated proteins from cell lysate using phosphate-affinity chromatography at physiological pHProteomics, 6, 5088-5095 (2006), E. Kinoshita-Kikuta, E. Kinoshita, A. Yamada, M. Endo, and T. Koike

  • Separation of a phosphorylated histidine protein using phosphate affinity polyacrylamide gel electrophoresis, Analytical Biochemistry360, 160-162 (2007), S. Yamada, H. Nakamura, E. Kinoshita, E. Kinoshita-Kikuta, T. Koike, and Y. Shiro

  • Label-free kinase profiling using phosphate-affinity polyacrylamide gel electrophresisMolecular & Cellular Proteomics, 6, 356-366 (2007), E. Kinoshita-Kikuta, Y. Aoki, E. Kinoshita, and T. Koike

  • A SNP genotyping method using phosphate-affinity polyacrylamide gel electrophoresis, Analytical Biochemistry361, 294-298 (2007), E. Kinoshita, E. Kinoshita-Kikuta, and T. Koike (The phosphate group at DNA-terminal is efficiently captured by Zn2+.Phos-tag.)

  • Identification on Membrane and Characterization of Phosphoproteins Using an Alkoxide-Bridged Dinuclear Metal Complex as a Phosphate-Binding Tag MoleculeJournal of Biomolecular Techniques18, 278-286 (2007), T. Nakanishi, E. Ando, M. Furuta, E. Kinoshita, E. Kikuta-Kinoshita, T. Koike, S. Tsunasawa, and O. Nishimura

  • A mobility shift detection method for DNA methylation analysis using phosphate affinity polyacrylamide gel electrophoresisAnalytical Biochemistry378, 102-104 (2008), E. Kinoshita-Kikuta, E. Kinoshita, and T. Koike

  • Separation of phosphoprotein isotypes having the same number of phosphate groups using phosphate- affinity SDS-PAGEProteomics, 8, 2994-3003 (2008), E. Kinoshita, E. Kinoshita-Kikuta, M. Matsubara, S. Yamada, H. Nakamura, Y. Shiro, Y. Aoki, K. Okita, and T. Koike

  • FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathwayNature Structural & Molecular Biology15, 1138-1146 (2008), M. Ishiai, H. Kitao, A. Smogorzewska, J. Tomida, A. Kinomura, E. Uchida, A. Saberi, E. Kinoshita, E. Kinoshita-Kikuta, T. Koike, S. Tashiro, S. J. Elledge, and M. Takata

  • to Page top

  • Two-dimensional phosphate affinity gel electrophoresis for the analysis of phosphoprotein isotypes Electrophoresis30, 550-559 (2009), E. Kinoshita, E. Kinoshita-Kikuta, M. Matsubara, Y. Aoki, S. Ohie, Y. Mouri, and T. Koike

  • Formation of lysophosphatidic acid, a wound-healing lipid, during digestion of cabbage leavesBioscience, Biotechnology, and Biochemistry,73, 1293-300 (2009), T. Tanaka, G. Horiuchi, M. Matsuoka, K. Hirano, A. Tokumura, T. Koike, and K. Satouchi

  • A Phos-tag-based fluorescence resonance energy transfer system for the analysis of the dephosphorylation of phosphopeptidesAnalytical Biochemistry388, 235-241, (2009), K. Takiyama, E. Kinoshita, E. Kinoshita-Kikuta, Y. Fujioka, Y. Kubo, and T. Koike

  • Phos-tag beads as an immunoblotting enhancer for selective detection of phosphoproteins in cell lysatesAnalytical Biochemistry389, 83-85, (2009), E. Kinoshita-Kikuta, E. Kinoshita, and T. Koike

  • Mobility shift detection of phosphorylation on large proteins using a Phos-tag SDS-PAGE gel strengthened with agaroseProteomics9, 4098- 4101 (2009), E. Kinoshita, E. Kinoshita-Kikuta, H. Ujihara, and T. Koike

  • Separation and detection of large phosphoproteins using Phos-tag SDS-PAGENature Protocols4, 1513-1521 (2009), E. Kinoshita, E. Kinoshita-Kikuta, and T. Koike

  • A clean-up technology for the simultaneous determination of lysophosphatidic acid and sphingosine-1-phosphate by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using a phosphate-capture molecule, Phos-tagRapid Communications in Mass Spectrometry24, 1075-1084 (2010), J. Morishige, M. Urikura, H. Takagi, K. Hirano, T. Koike, T. Tanaka, and K. Satouchi

  • Genotyping and mapping assay of single-nucleotide polymorphisms in CYP3A5 using DNA-binding zinc(II) complexesClinical Biochemistry43, 302-306 (2010), E. Kinoshita, E. Kinoshita-Kikuta, H. Nakashima, and T. Koike

  • The DNA-binding activity of mouse DNA methyltransferase 1 is ragulated phosphorylation with casein kinase 1σ/εBiochemical Journal427, 489-497 (2010), Y. Sugiyama, N. Hatano, N. Sueyoshi, I. Suetake, S. Tajima, E. Kinoshita, E. Kinoshita-Kikuta, T. Koike, and I. Kameshita


康宁corning 3505 PLT,96W,WHT,PSW/0.2u PVDF MEMB 96孔FiltrEX滤板 白色 PS(聚苯乙烯) 0.2um孔径PVDF(聚偏氟乙烯)亲水膜 灭菌 10个/包

康宁corning 3505 PLT,96W,WHT,PSW/0.2u PVDF MEMB
96孔FiltrEX滤板 白色 PS(聚苯乙烯) 0.2um孔径PVDF(聚偏氟乙烯)亲水膜 灭菌 10个/包 5包/箱 16378.8

日立氨基酸分析仪配套试剂(适用于L-8500型,L-8900型)

上海金畔生物科技有限公司提供日立氨基酸分析仪配套试剂(适用于L-8500型,L-8900型)

 日立氨基酸分析仪配套试剂的选择:

日立氨基酸分析仪在国内使用较为普遍,现国内使用的型号主要为L-8500型,L-8500A型,L-8800型,L-8900型等,在选择他们的配套试剂时,有很多人非常的迷惑,希望以下的能帮助您!

日立本身并不生产试剂,其仪器的配套都是由日本的两家大型化学试剂生产商为其配套生产。不论是什么型号的配套试剂,基本都分3部分:

  1. 缓冲液
  2. 再生液
  3. 显色液

日立前期推出的氨基酸分析仪包括835型,L-8500型,L-8500A型,L-8800型等配套试剂都有分PH和PF系列,两者适用于不同的样本:

PH系列: 蛋白质水解产物分析

PF系列: 生物液体分析

L-8900型可以使用L-8500型的配套试剂,但是如果希望具有高吞吐能力,则需要使用L-8900型专用的配套试剂L-8900型PFS系列。

PFS系列: 生物液体分析,相比PF具有高吞吐能力

 

所以主流的日立氨基酸分析仪配套试剂为L-8500型PH系列、L-8500型PF系列、L-8900型PFS系列。

如果您的仪器是L-8500型,L-8500A型,L-8800型,样本为蛋白质水解产物时,适合使用以下配套试剂:

608-07461    MCI Buffer L-8500-PH Kit      1KIT (包含:PH-1 1L*2, PH-2 1L*1, PH-3 1L*1, PH-4 1L*2, PH-RG 1L*1)

634-12471    MCI Buffer L-8500-PH-1      1L×2

604-07463    MCI Buffer L-8500-PH-1      1L×10

608-07466    MCI Buffer L-8500-PH-2      1L×10

631-12481    MCI Buffer L-8500-PH-2      1L×2

606-07462    MCI Buffer L-8500-PH-3      1L×10

638-12491    MCI Buffer L-8500-PH-3      1L×2

631-12501    MCI Buffer L-8500-PH-4      1L×2

602-07464    MCI Buffer L-8500-PH-4      1L×10

638-12511    MCI Buffer L-8500-PH-RG      1L×2

600-07465    MCI Buffer L-8500-PH-RG      1L×10

299-70501    NINHYDRIN COLORING SOLUTION KIT FOR HITACHI FOR2L

 

如果您的仪器是L-8500型,L-8500A型,L-8800型,样本为生物液体,适合使用以下配套试剂:

605-07471    MCI Buffer L-8500-PF Kit      1KIT (包含:PF-1 1L*2, PF-2 1L*1, PF-3 1L*1, PF-4 1L*2, PF-RG 1L*1)

601-07473    MCI Buffer L-8500-PF-1      1L×10

639-12421    MCI Buffer L-8500-PF-1      1L×2

607-07475    MCI Buffer L-8500-PF-2      1L×10

636-12431    MCI Buffer L-8500-PF-2      1L×2

633-12441    MCI Buffer L-8500-PF-3      1L×2

605-07476    MCI Buffer L-8500-PF-3      1L×10

630-12451    MCI Buffer L-8500-PF-4      1L×2

609-07474    MCI Buffer L-8500-PF-4      1L×10

603-07472    MCI Buffer L-8500-PF-RG      1L×10

637-12461    MCI Buffer L-8500-PF-RG      1L×2

299-70501    NINHYDRIN COLORING SOLUTION KIT FOR HITACHI FOR2L

 

如果您的仪器是L-8900型,不需要高吞吐能力时,可以使用L-8500系列的试剂(样本为蛋白质水解产物使用PH系列,样本为生物液体使用PF系列,显色液使用NINHYDRIN COLORING SOLUTION KIT FOR HITACHI)

如果您的仪器是L-8900型,且需要高吞吐能力时,适合使用以下配套试剂:

632-07401     MCI Buffer L-8900 PFS KIT      1KIT (包含:PFS-1 1L*2、PFS-2 1L*2、PFS-3 1L*1、PFS-4 1L*1、PFS-RG 1L*1)

639-07411     MCI Buffer L-8900 PFS-1      1L×10

636-07421     MCI Buffer L-8900 PFS-2      1L×10

633-07431     MCI Buffer L-8900 PFS-3      1L×10

630-07441     MCI Buffer L-8900 PFS-4      1L×10

637-07451     MCI Buffer L-8900 PFS-RG      1L×10

299-70501    NINHYDRIN COLORING SOLUTION KIT FOR HITACHI FOR2L

更多产品,更多优惠,请联系我们!
上海金畔生物科技有限公司
订货热线:15221999938
网 址: www.jinpanbio.com
金畔博客:www.jinpanbio.cn
Email:sales@jinpanbio.com

 

原装进口英国Whatman6809-2002Anotop针头式滤器 ANOTOP 25/0.02 50/PK

原装进口英国Whatman6809-2002Anotop针头式滤器 ANOTOP 25/0.02 50/PK

 

 

 

 




产品介绍:

Anotop针头式滤器

Anotop™针头式滤器用于于大多数的有机溶液和水溶液,最

大过滤量可达100 ml。这个滤器的特点是有一个很明显的六

边形外壳,由无色聚丙烯材料制成,避免了样品的污染,在

生产过程中不添加任何润湿剂或添加剂。

 

Anotop针头式滤器中含有唯一的Anopore铝膜,有3种孔径可

选。玻璃微纤维预滤层适合于难过滤样品。

 

Anotop 10

特点

l 10 mm直径针头式滤器

l 无机膜

l 毛细管状孔结构

 

优点

l 蛋白吸附力低

l 过滤样品量达10 ml

l 样品吸附量低< 20μl,保证了样品的最大回收量

l 对于一些重要的应用,有无菌包装供您选择

 

Anotop 10 Plus

Anotop 10 Plus针头式滤器增加了一套完整的玻璃微纤维预

滤层。这种滤器设计用来过滤难过滤的样品,对终滤层滤膜

的过滤效率没有任何负面影响,从而就减少了澄清样品所需

要花费的时间和费用。

 

应用

l HPLC之前,高粒子含量样品的过滤

l UV/可见光分析前,固体物的去除



      Anotop10

Anotop 10 and Anotop 25

Anotop 25

特点

l 25 mm直径的针头式滤器

l 样品过滤量达100 ml

 

应用

l 生长介质的冷消毒

l 噬菌体和病毒的过滤

l 去除高分子量蛋白或聚合物

l 脂质体挤压

l 光谱分析的溶液的过滤,以及分析样品的准备

 

Anotop 25 Plus

Anotop 25 Plus针头式滤器增加了一套完整的玻璃微纤维预

滤层。这种滤器设计用来过滤难过滤的样品,对终滤层滤膜

的过滤效率没有任何负面影响,从而减少了澄清样品所需要

花费的时间和费用。

 

应用

l 组织培养基的过滤

l 难过滤样品的纯化

l 胶体材料的过滤

l 去除支原体的

l HPLC样品准备

l 生物样品制备

 

Anotop IC

Whatman Anotop IC针头式滤器专们为用于后续离子色谱法

和HPLC分析的样品制备而设计。这种滤器保证了离子色谱

法测定中阴离子过滤的低水平。

 

特点

l 10 mm直径针头式滤器

l 25 mm直径针头式滤器

l 不同批次有IC认证

 

优点

l 分析结果有更好的一致性

l 延长了柱子的寿命

l 经认证,保证低水平的阴离子过滤,意味着结果会更好

 

应用

l 离子色谱法样品准备

l HPLC样品制备

 

Anotop LC

Whatman Anotop LC针头式滤器专们为HPLC分析前的样品简

单有效的制备而设计。这种滤器通过从分析样品中有效的去

处颗粒延长了柱子的使用寿命。由于Anotop LC针头式滤器

由无色聚丙烯制成并使用了Anopore无机膜,可以确保过滤

后提取紫外吸收物水平最小化。

 

特点

l 分析结果更好的一致性和更长的柱使用寿命

l 极低的紫外吸收物水平意味着更好的HPLC结果

l 易于与所有样品类型使用

 

            Anotop LC


 

合成·反应装置ケミスト广场CPP – 2000系列用1 / 4用螺母10个入|柴田科技有限公司-环境检测设备、科学仪器的制造销售

产品详细

科学仪器

合成·反应装置ケミスト广场CPP – 2000系列用1 / 4用螺母10个入

商品代码其他情报(式样)

这个产品比较表中追加
商品代码 054310 – 2746 A
型式
价格(不含税) 5,400日元

上海金畔生物科技有限公司

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