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VCAM1蛋白,VCAM1
  • VCAM1蛋白,VCAM1
  • VCAM1蛋白,VCAM1
  • VCAM1蛋白,VCAM1

VCAM1重組蛋白 GMP級別,ACROBiosystems百普賽斯

價格 詢價
包裝 100ug 500ug 1000ug
最小起訂量 100ug
發(fā)貨地 北京
更新日期 2024-12-16
微信洽談

產(chǎn)品詳情

中文名稱:VCAM1蛋白英文名稱:VCAM1
品牌: 百普賽斯產(chǎn)地: 北京
保存條件: -20°C to -70°C純度規(guī)格: 99.9%
產(chǎn)品類別: 重組蛋白
貨號: VCAM1用途范圍: 藥物開發(fā)等
規(guī)格: 100ug是否進口:
2024-12-16 VCAM1蛋白 VCAM1 100ug/RMB;500ug/RMB;1000ug/RMB 百普賽斯 北京 -20°C to -70°C 99.9% 重組蛋白

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VCAM1產(chǎn)品信息

英文名稱Vascular cell adhesion molecule 1

中文名稱:血管細胞粘附分子1

靶點別稱VCAM1,CD106,INCAM-100,V-CAM 1,VCAM-1

物種:Human

標簽His Tag / Fc Tag / Fc Tag & Avi Tag

屬性:Protein

標記:Biotin-labeled / Unconjugated

優(yōu)勢特色(Features

1. Designed under ISO 9001:2015 and ISO 13485:2016

2. Manufactured and QC tested under a GMP compliance factory

3. Animal-Free materials

4. Batch-to-batch consistency

5. Stringent quality control tests

表達區(qū)間及表達系統(tǒng)(Source

GMP Human VCAM-1 Protein, Fc Tag (GMP-VC1H25) is expressed from human 293 cells (HEK293). It contains AA Phe 25 - Glu 698 (Accession # P19320-1 ).

Predicted N-terminus: Phe 25

蛋白結(jié)構(gòu)(Molecular Characterization

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This protein carries a human IgG1 Fc tag at the C-terminus.

The protein has a calculated MW of 100.7 kDa.

無菌(Sterility

The sterility testing was performed by membrane filtration method described in CP<1101>, USP<71>and Eur. Ph. 2.6.1.

制劑(Formulation

Please contact us for detailed information.

Contact us for customized product form or formulation.

重構(gòu)方法(Reconstitution

Please see Certificate of Analysis for specific instructions.

For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.

存儲(Storage

Shipping at ambient temperature. Upon receipt, store it immediately at -20°C or lower for long term storage.

Please avoid repeated freeze-thaw cycles.

This product is stable after storage at:

1. -20°C to -70°C for 5 years in lyophilized state;

2. -70°C for 12 months under sterile conditions after reconstitution.

MANUFACTURING SPECIFICATIONS

ACROBiosystems GMP grade products are produced under a quality management system and in compliance with relevant guidelines: Ph. Eur General Chapter 5.2.12 Raw materials of biological origin for the production of cell-based and gene therapy medicinal products; USP<92>Growth Factors and Cytokines Used in Cell Therapy Manufacturing; USP<1043>Ancillary Materials for Cell, Gene, and Tissue-Engineered Products; ISO/TS 20399-1:2018, Biotechnology - Ancillary Materials Present During the Production of Cellular Therapeutic Products.

ACROBiosystems Quality Management System Contents

1. Designed under ISO 9001:2015 and ISO 13485:2016, Manufactured and QC tested under a GMP compliance factory.

2. Animal-Free materials

3. Materials purchased from the approved suppliers by QA

4. ISO 5 clean rooms and automatic filling equipment

5. Qualified personnel

6. Quality-related documents review and approve by QA

7. Fully batch production and control records

8. Equipment maintenance and calibration

9. Validation of analytical procedures

10. Stability studies conducted

11. Comprehensive regulatory support files

ACROBiosystems provide rigorous quality control tests (fully validated equipment, processes and test methods) on our GMP grade products to ensure that they meet stringent standards in terms of purity, safety, activity and inter-batch stability, and each bulk QC lot mainly contains the following specific information:

1. SDS-PAGE

2. Protein content

3. Endotoxin level

4. Residual Host Cell DNA content

5. Residual Host Cell Protein content

6. Biological activity analysis

7. Microbial testing

8. Mycoplasma testing

9. In vitro virus assay

10. Residual moisture

11. Batch-to-batch consistency

DISCLAIMER

ACROBiosystems GMP grade products are designed for research, manufacturing use or ex vivo use. CAUTION: Not intended for human in vivo applications.

TERMS AND CONDITIONS

All products are warranted to meet ACROBiosystems Inc.’s (“ACRO”) published specifications when used under normal laboratory conditions.

ACRO DOES NOT MAKE ANY OTHER WARRANTY OR REPRESENTATION WHATSOEVER, WHETHER EXPRESS OR IMPLIED, WITH RESPECT TO ITS PRODUCTS. IN PARTICULAR, ACRO DOES NOT MAKE ANY WARRANTY OF SUITABILITY, NONINFRINGEMENT, MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR PURPOSE.

NOT WITH STANDING ANY OTHER PROVISIONS OF THESE TERMS AND/OR ANY OTHER AGREEMENT BETWEEN ACRO AND PURCHASER FOR THE PURCAHSE OF THE PRODUCTS, ACRO’S TOTAL LIABILITY TO PURCHASER ARISING FROM OR IN RELATION TO THESE TERMS, AN AGREEMENT BETWEEN THE PARTIES OR THE PRODUCTS, WHETHER ARISING IN CONTRACT, TORT OR OTHERWISE SHALL BE LIMITED TO THE TOTAL AMOUNT PAID BY PURCHASER TO ACRO FOR THE RELEVANT PRODUCTS. IN NO EVENT WILL ACRO BE LIABLE FOR THE COST OF PROCUREMENT OF SUBSTITUTE GOODS.

END USER TERMS OF USE OF PRODUCT

The following terms are offered to you upon your acceptance of these End User Terms of Use of Product. By using this product, you indicate your acknowledgment and agreement to these End User Terms of Use of Product. If you do not agree to be bound by and comply with all of the provisions of these End User Terms of Use of Product, you should contact your supplier of the product and make arrangements to return the product.

The End User is aware that ACROBiosystems Inc. and its affiliate (“ACRO”) sell GMP grade products designed for research, manufacturing use or ex vivo use and not intended for human in vivo applications. The End User further agrees, as a condition of the sales of ACRO’s GMP grade products that: a) the End User will not use this GMP grade product in any procedure wherein the product may be directly or indirectly administered to humans, unless the End User has obtained, or prior to their use will have obtained, an Investigational New Drug (IND) exemption from the FDA and will use the product only in accordance with the protocols of such IND and of the Institutional Review Board overseeing the proposed research, or b) the End User will use the products outside of the United States in accordance with the protocols of research approved by the applicable review board or authorized ethics committee and regulatory agencies to which the End User is subject to in their territory.

VCAM1分子背景

血管細胞粘附蛋白1VCAM-1)也稱為CD106INCAM-100L1CAM,是一種屬于免疫球蛋白超家族的細胞表面唾液酸糖蛋白。VCAM-1/CD106含有7IgC2型(免疫球蛋白樣)結(jié)構(gòu)域。CD106/VCAM-1在炎癥的血管內(nèi)皮細胞上表達,在正常和炎癥組織中的巨噬細胞樣細胞和樹突狀細胞類型上也表達。L1CAM/VCAM-1在細胞識別中很重要,似乎在白細胞-內(nèi)皮細胞粘附中起作用。CD106/VCAM-1與白細胞上的β-1整合素VLA4相互作用,介導(dǎo)粘附和信號轉(zhuǎn)導(dǎo)。VCAM-1/VLA4相互作用可能在免疫反應(yīng)和白細胞向炎癥部位遷移中發(fā)揮病理生理作用。INCAM-100/VCAM1ECMV-D衣殼蛋白結(jié)合,并作為該病毒的受體。


關(guān)鍵字: VCAM1;VCAM1蛋白;血管細胞粘附分子1;CD106;CD106蛋白;

公司簡介

百普賽斯集團ACROBiosystems Group(股票代碼:301080)是成立于2010年的跨國生物科技公司,是為全球生物醫(yī)藥、健康產(chǎn)業(yè)領(lǐng)域提供關(guān)鍵生物試劑產(chǎn)品及解決方案的行業(yè)平臺型基石企業(yè)。2021年在創(chuàng)業(yè)板上市。百普賽斯集團業(yè)務(wù)遍布全球,橫跨亞洲、北美洲、歐洲,在中國、美國、瑞士等12個城市設(shè)有辦公室、研發(fā)中心及生產(chǎn)基地。目前累計服務(wù)客戶超6000家,與全球Top 20醫(yī)藥企業(yè)均建立了長期、穩(wěn)定的合作伙伴關(guān)系。集團旗下?lián)碛衅放艫CROBiosystems百普賽斯、bioSeedin柏思薈、Condense Capital墾拓資本和ACRODiagnostics百斯醫(yī)學(xué)等。
成立日期 2010-07-22 (15年) 注冊資本 8000萬人民幣
員工人數(shù) 500人以上 年營業(yè)額 ¥ 1億以上
主營行業(yè) 醫(yī)藥中間體,原料藥,激素類,氨基糖苷類,中樞神經(jīng)系統(tǒng)用藥 經(jīng)營模式 工廠,試劑
  • 北京百普賽斯生物科技股份有限公司
VIP 2年
  • 公司成立:15年
  • 注冊資本:8000萬人民幣
  • 企業(yè)類型:其他股份有限公司(上市)
  • 主營產(chǎn)品:重組蛋白,抗原,抗體,試劑盒
  • 公司地址:北京市北京經(jīng)濟技術(shù)開發(fā)區(qū)宏達北路8號4幢4層
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