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GMP級(jí)別白介素15,GMP Human IL-15
  • GMP級(jí)別白介素15,GMP Human IL-15
  • GMP級(jí)別白介素15,GMP Human IL-15
  • GMP級(jí)別白介素15,GMP Human IL-15

GMP級(jí)別IL-15蛋白-ACROBiosystems百普賽斯

價(jià)格 5000 20000 35000
包裝 50ug 500ug 1000ug
最小起訂量 50ug
發(fā)貨地 北京
更新日期 2024-11-12
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產(chǎn)品詳情

中文名稱:GMP級(jí)別白介素15英文名稱:GMP Human IL-15
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(hào): GMP Human IL-15用途范圍: 藥物開(kāi)發(fā)等
規(guī)格: 100ug是否進(jìn)口:
2024-11-12 GMP級(jí)別白介素15 GMP Human IL-15 50ug/5000RMB;500ug/20000RMB;1000ug/35000RMB 5000 百普賽斯 北京 -20°C to -70°C 99.9% 重組蛋白

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GMP Human IL-15 Protein

優(yōu)勢(shì)特色(Features

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

2. Manufactured and QC tested under a GMP compliance factory

3. FDA DMF filed

4. Animal-Free materials

5. Batch-to-batch consistency

6. Stringent quality control tests

7. No animal derived peptone and lactose used in production process

表達(dá)區(qū)間及表達(dá)系統(tǒng)(Source

GMP Human IL-15 Protein (GMP-L15H13) is expressed from E. coli cells. It contains AA Asn 49 - Ser 162 (Accession # P40933-1 ).

Predicted N-terminus: Met

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

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This protein carries no "tag".

The protein has a calculated MW of 12.8 kDa. The protein migrates as 13 kDa±3 kDa under reducing (R) condition (SDS-PAGE).

內(nèi)毒素(Endotoxin

Less than 10 EU/mg by the LAL method.

宿主蛋白殘留(Host Cell Protein

<0.5 ng/μg of protein tested by ELISA.

宿主核酸殘留(Host Cell DNA

<0.02 ng/μg of protein tested by DNA Fluorescent Staining method.

無(wú)菌(Sterility

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

支原體(Mycoplasma

Negative.

外源病毒(In vitro virus assay

Negative

純度(Purity

>95% as determined by SDS-PAGE.

制劑(Formulation

Lyophilized from 0.22 μm filtered solution in 25 mM His, pH6.2 with protectants.

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(chǔ)(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.

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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 direct human use.

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.

GMP Human IL-15用戶評(píng)價(jià)

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關(guān)鍵字: IL-15;白介素15;GMP Human IL-15;GMP IL-15;GMP白介素15;

公司簡(jiǎn)介

百普賽斯集團(tuán)ACROBiosystems Group(股票代碼:301080)是成立于2010年的跨國(guó)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(tái)型基石企業(yè)。2021年在創(chuàng)業(yè)板上市。百普賽斯集團(tuán)業(yè)務(wù)遍布全球,橫跨亞洲、北美洲、歐洲,在中國(guó)、美國(guó)、瑞士等12個(gè)城市設(shè)有辦公室、研發(fā)中心及生產(chǎn)基地。目前累計(jì)服務(wù)客戶超6000家,與全球Top 20醫(yī)藥企業(yè)均建立了長(zhǎng)期、穩(wěn)定的合作伙伴關(guān)系。集團(tuán)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(cè)資本 8000萬(wàn)人民幣
員工人數(shù) 500人以上 年?duì)I業(yè)額 ¥ 1億以上
主營(yíng)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(yíng)模式 工廠,試劑
  • 北京百普賽斯生物科技股份有限公司
VIP 1年
  • 公司成立:15年
  • 注冊(cè)資本:8000萬(wàn)人民幣
  • 企業(yè)類型:其他股份有限公司(上市)
  • 主營(yíng)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(jì)技術(shù)開(kāi)發(fā)區(qū)宏達(dá)北路8號(hào)4幢4層
詢盤(pán)

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