當(dāng)前位置 ： Moregate >>> Moregate/Adult Bovine Serum - Raw (ABSR)/null/ABSR
Moregate/Adult Bovine Serum - Raw (ABSR)/null/ABSR
  • Moregate/Adult Bovine Serum - Raw (ABSR)/null/ABSR

Moregate/Adult Bovine Serum - Raw (ABSR)/null/ABSR

價(jià)格: ￥10.00 市場(chǎng)價(jià): 20.00
貨號(hào): ABSR
品牌: Moregate
規(guī)格
數(shù)量
庫存(0)
特別 提示
代購產(chǎn)品：無質(zhì)量問題不接受退換貨，下單前請(qǐng)仔細(xì)核對(duì)信息。
下單后請(qǐng)及時(shí)聯(lián)系客服核對(duì)商品價(jià)格，訂單生效后再付款。
資深產(chǎn)品顧問
咨詢顧問

全國免費(fèi)服務(wù)熱線

4000-520-616

  • 自營商城 一站式服務(wù)
  • 廠家直采 剔除溢價(jià)
  • 品質(zhì)甄選 正品保證
  • 嚴(yán)控流程 只做188精品
  • 極速物流 如約送貨
  • 詳情
  • 使用說明
  • 常見問題

    • Adult Bovine Serum – Raw (ABSR), is obtained from blood taken from cattle deemed fit for human consumption following ante and post mortem veterinary inspection.? The blood is collected in slaughter-houses supervised by government veterinarians.?

      The blood is collected in lined sanitary buckets and allowed to clot naturally without the addition of any clotting factors. The blood is then transferred to a temperature controlled clean environment where the liquid component of the blood is drained and separated using a continuous flow separator before being dispensed into 5L Bottles and immediately frozen.?

      SPECIFICATION - Adult Bovine Serum - RAW (ABSR)
      ProductAdult Bovine Serum - Raw
      Catalogue No.ABSR
      Certificate of SuitabilityNew Zealand R1-CEP2001-093
      SourceBovine blood from healthy animals which have been inspected ante and post mortem by Australian or New Zealand Government veterinarians and passed as fit for human consumption.
      Collection MethodBlood is collected into sanitary containers. Serum is produced in temperature controlled conditions.The blood is drained and separated using a continuous flow separator. It is then immediately frozen.
      IrradiationIrradiation can be performed on request
      Pack Size5 Litre container or to Customer Specifications
      Storage-20 degrees Centigrade
      Expiry DateSix years from the date of manufacture
      TestMethodSpecification
      Aerobic Microbial CountCFU/ml< 1000 CFU/mL

      EP/USP

      The European Pharmacopeia consists of a number of general and specific monographs covering various classes of products.

      The monographs set out requirements to be met and followed for all products in the class.

      Recently the EP has introduced a Monograph for Bovine Serum – Monograph No 04/2006:2262 to be found in E.P. 5.4

      This monograph provides a definition of Bovine Serum and sets out details of production, and requirements for viral inactivation parameters, quality control testing, storage conditions and labelling.

      Moregate Bovine Serum products meet these requirements and Certificates of Analysis are modeled on the QC test requirements.

      ?

      The United States Pharmacopeia-National Formulary (USP-NF) contains standards for medicines, dosage forms, drug substances, excipients, medical devices, and dietary supplements.

      Within the Pharmacopeia are Monographs and general chapters.

      The monographs consist of information such as the ingredient name, definition, packaging and labelling requirements, storage and a specification.

      The specifications list tests to be performed along with the procedure to be followed and the acceptable limit.

      EMEA/CPMP/CVMP

      The European Medicines Agency (EMEA) is a decentralised body of the European Union with headquarters in London. It sits alongside the European Directorate for the Quality of Medicines (EDQM).

      The main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use.

      The EMEA publishes guidelines on quality, safety and efficacy testing requirements.

      These guidelines are prepared by committees, and those guidelines which relate to the use of Bovine Serum, including Fetal Bovine Serum, in the manufacture of medicines include:

      CPMP: Committee for Proprietary Medicinal Products

      Note for Guidance on the Use of Bovine Serum in the Manufacture of Human Biological Medicinal Products

      Note for Guidance on Minimising the Risk of Transmitting Animal Spongiform Encephalopathy Agents via Human and Veterinary Medicinal Products. (Also adopted by the CVMP)

      CVMP: Committee for Veterinary Medicinal Products

      Requirements and Controls applied to Bovine Serum used in the production of Immunological Veterinary Medicinal products.

      These Guidelines include requirements for Virus Testing of Fetal Bovine Serum and other Bovine Serum. Further reference to these requirements can be found in “Virus Testing”.?

      All Moregate Biotech Fetal Bovine Serum and other Bovine Serum meet the requirements of the Guidelines in relation to Fetal Bovine Serum and Bovine Serum.

      USDA 9CFR Part 113.53c

      Ingredients of animal origin used in the United States of America, in the manufacture of veterinary and human biologics are required to be in compliance with the Code of Federal Regulations, Title 9 – Animals and Animal Products, Chapter 1 - Animal and Plant Health Inspection Service, Department of Agriculture Part 113-53c, commonly referred to as 9CFR Part 113-53c.

      This legislation sets out the requirements for detection of extraneous viruses, detailing the methods to be used and the list of viruses that shall be tested for. ?

      Over time 9CFR Part 113-53c became the accepted standard for the testing of animal sera, particularly Fetal Bovine Serum for adventitious viral agents.

      Bovine Respiratory Syncytical Virus, Bovine Viral Diarrhea Virus, Bovine Parvovirus, Bluetongue Virus, Bovine Adenovirus, Rabies Virus and Reovirus are tested for by fluorescent antibody

      Infections Bovine Rhinotracheitis tested for by Cytopathic Agents.

      Infectious Influenza 3 tested for by Haemadsorbing Agents

      EDQM

      The European Directorate for the Quality of Medicines (EDQM) has originated from the European Pharmacopoeia Secretariat which, with the addition of new responsibilities changed its name to the European Department for the Quality of Medicines (EDQM).? The EDQM sits alongside the European Medicines Agency (EMEA).

      Amongst other activities, the EDQM is responsible for the European Pharmacopeia and the issuing of Certificates of Suitability (CEP).

      Certificates of Suitability (CEP) are?recognised?by all signatory states of the European Pharmacopoeia Convention and by the European Union. Other countries have also chosen to recognise them.? In the case of Fetal Bovine Serum and other Bovine Serum a CEP can be used by the manufacturers of Fetal Bovine Serum and other Bovine Serum which is intended for use in the manufacture of pharmaceutical products to demonstrate compliance with the Bovine Serum monographs of the European Pharmacopoeia and the EDQM requirements for substances concerned by TSE risk.

      The discovery of Bovine Spongiform Encephalopathy (BSE), which is one of a group of similar infections now referred to as Transmissible Spongiform Encephalopathies (TSEs), and it’s spread over many countries of the European Union as well as its discovery in Canada, the USA and Japan is well known. The European events provided the impetus for the Council of Europe Public Health Committee (CEPHC) to pass Resolution AP-CSP (99) 5 addressing the TSE concerns and creating a Certificate of Suitability (COS) pursuant to Directive 75/318/EEC.

      The granting of a CoS to a manufacturer, for a particular product, certifies that the product in question has been assessed for the level of risk of transmission of TSEs, and that the risk level is considered low enough that the product is certified as suitable for use in the manufacture of medicinal products in the European Union.

      The process of approval requires the manufacturer to submit a dossier that covers all relevant aspects of the collection of raw material and further processing that is performed to reach the product that is offered to end users. This dossier is detailed and covers the specific material that is collected, the collection method, process validation, testing, traceability, quality systems and an expert review.

      Only after this dossier has been examined and approved by two rapporteurs and, if necessary, by a panel of experts appointed by the European Directorate for the Quality of Medicines (EDQM) is the manufacturer granted a COS. ??

      Moregate Biotech has been granted a COS for:

      ?? ?- Fetal Bovine Serum – Australian Origin – CEP2000-187
      ?? ?- Fetal Bovine Serum – New Zealand Origin – CEP2000-188
      ?? ?- Adult Bovine Serum - New Zealand Origin – CEP2001-093
      ?? ?- Adult Bovine Serum (Defibrinated) - New Zealand Origin – CEP2000-174
      ?? ?- Bovine Plasma – New Zealand Origin – CEP2003-199
      ?? ?- Bovine Serum Albumin – manufactured in Australia from New Zealand origin Bovine Plasma – CEP2003-205
      ?? ?- Bovine Plasma – Australian Origin - CEP 2005-192
      ?? ?- Bovine Serum Albumin – manufactured in Australia from Australian origin Bovine Plasma - CEP 2005-191
      Copies of the Certificates of Suitability are available upon request

      Hazards Identification

      • Not hazardous
      • Get Medical attention immediately

      First Aid Measures
      Get Medical attention immediately.

      Ingestion
      If swallowed, give several glasses of water to drink to dilute.

      Skin Contact
      Wash skin with soap and copious amounts of water.

      Eye Contact
      Flush with water for at least 15 minutes, lifting upper and lower eyelids occasionally.

      Accidental Release

      Procedures for Personal Precaution
      Exercise appropriate precautions to minimize direct contact with skin or eyes.

      Methods for Cleaning Up
      Mop up
      Ventilate area and wash spill site after material pickup is complete

      Handling and Storage

      Handling
      Normal measures for preventive fire protection

      Storage
      Keep tightly closed under correct storage conditions

      Exposure Controls / Personal Protection

      • Wash thoroughly after handling.
      • Protective gloves

      Disposal Considerations
      Contact a licensed professional waste disposal service to dispose of this material.

      Transport Information

      • Non-hazardous for road transport
      • Non-hazardous for sea transport
      • Non-hazardous for air transport

      Note: The above information is believed to be correct, but shall be used as a guide only.

      Disclaimer: For pharmaceutical use only.
    售后保障
    螞蟻淘生物188，秉承螞蟻淘一貫的嚴(yán)謹(jǐn)態(tài)度，由螞蟻淘公司專業(yè)人員負(fù)責(zé)品控、采購、物流、銷售、售后，保障正品優(yōu)質(zhì)。以“快速好省，為科研提供好產(chǎn)品、好價(jià)格”為理念，直接鏈接原廠家，從全國各地原制造商嚴(yán)格挑選188款科研精品，剔除品牌溢價(jià)，188生物新電商，把好的產(chǎn)品帶給科研！? 力求給你最優(yōu)質(zhì)的商品。
  • Q：生物188產(chǎn)品正品保障嗎？
    A：生物188質(zhì)量把控人員具有十年的從業(yè)經(jīng)驗(yàn)，在業(yè)界享有良好的口碑；自營商城，直接從廠家采購， 自己的團(tuán)隊(duì)負(fù)責(zé)國際物流和清關(guān)，中間沒有第三方，所有流程嚴(yán)格把控，100%保證正品，假一罰十。

    Q：下單后可以修改訂單嗎？
    A：下單后的商品付款之前可以修改；訂單付款成功，需要聯(lián)系我們客服進(jìn)行修改；客服電話：4000-520-616

    Q：可以開發(fā)票嗎？
    A：本網(wǎng)站所售商品都是正規(guī)清關(guān)，均開具16%正規(guī)發(fā)票，發(fā)票金額含配送費(fèi)金額，另有說明的除外。

    Q：商品幾天可以發(fā)貨？
    A：生物188商品，全部現(xiàn)貨銷售，付款后即可發(fā)貨,一般一周內(nèi)送達(dá)！

    Q：如何聯(lián)系商家？
    A：有任何問題夠可以電話咨詢我們，全國24小時(shí)免費(fèi)服務(wù)熱線：4000-520-616 或聯(lián)系我們的在線客服QQ：1570468124

    Q：收到的商品少了/發(fā)錯(cuò)了怎么辦？
    A：同個(gè)訂單購買多個(gè)商品可能會(huì)分為一個(gè)以上包裹發(fā)出，可能不會(huì)同時(shí)送達(dá)，建議查看訂單詳情是否是 部分發(fā)貨狀態(tài)；如未收到，可聯(lián)系在線客服或者致電4000-520-616。

    Q：退換貨/維修需要多長時(shí)間？
    A：一般情況下，退貨處理周期為客戶收到產(chǎn)品一個(gè)月內(nèi)（以快遞公司顯示簽收時(shí)間為準(zhǔn)），包裝規(guī)格、 數(shù)量、品種不符，外觀毀損、短缺或缺陷，請(qǐng)?jiān)谑盏截?4小時(shí)內(nèi)申請(qǐng)退換貨；特殊商品以合同條款為準(zhǔn)。

何為188

極簡而嚴(yán)謹(jǐn)，我們僅銷售188款生物醫(yī)學(xué)科研用品，款款都是爆款；因?yàn)樯偎跃劢梗劢拐邕x每一款產(chǎn)品，聚焦服務(wù)每一位客戶!

關(guān)注我們 :

點(diǎn)擊QQ聯(lián)系我們
生物188微信

關(guān)注188微信公眾號(hào)

獲取最新優(yōu)惠活動(dòng)通知