다음 MAP메이트™는 통합될 수 없습니다: -다른 분석 완충용액이 필요한 MAP메이트™. -인산 특이성 및 총 MAP메이트™ 조합, 예: 총 GSK3β 및 GSK3β(Ser 9). -PanTyr 및 자리 특이성 MAP메이트™, 예: Phospho-EGF 수용체 및 phospho-STAT1(Tyr701). -단일 표적(Akt, STAT3)를 위한 1개 이상의 1 phospho-MAP메이트™. - GAPDH 및 β-Tubulin은 panTyr를 포함하는 키트 또는 MAP메이트™와 통합될 수 없습니다.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
Catalogue Number
Ordering Description
Qty/Pack
List
이 제품은 즐겨찾기에 저장되었습니다.
종
패널 유형
선택하신 키트
수량
카탈로그 번호
주문 설명
포장 단위
기재 가격
96-Well Plate
수량
카탈로그 번호
주문 설명
포장 단위
기재 가격
다른 시약 추가 (MAP메이트 사용을 위해 완충용액과 검출 키트가 필요함)
수량
카탈로그 번호
주문 설명
포장 단위
기재 가격
48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
공간 절약 옵션 다수의 키트를 구매하시는 고객은 고용량 저장을 위해 키트 포장을 제거하고 비닐백에 담긴 멀티플레스 분석 구성품을 받아 저장 공간을 절약하도록 선택할 수 있습니다.
이 제품은 즐겨찾기에 저장되었습니다.
해당 제품은 고객님의 카트에 추가되었습니다.
이제 다른 키트를 사용자 지정하거나, 사전 혼합된 키트를 선택하거나, 결재하거나 또는 주문 도구를 종료할 수 있습니다.
To comply with GMP guidelines worldwide and the US Code of Federal Regulations, physical and chemical compatibility testing is necessary to prove that filters and single-use systems used in biopharmaceutical manufacturing are not reactive, additive or absorptive when they come into contact with drug product.
With more than 100 dedicated engineers and technicians, we are able to offer unparalleled expertise in every area of your manufacturing process, getting you from gene to clinic in less than 12 months.
As a manufacturer of pharmaceutical active substances and excipients, food additives and other food ingredients as well as active cosmetic substances, Merck operates according to recognized international quality standards and relevant regulations.
... validated cGMP-conform system. Effects transport using cGMP-tested forwarding companies. Afrees to change-control-processes with its customers. Compiles comprehensive product documentation. Download our GMP statements: GMP for API GMP for Excipients...
An Easy-to-Use GMP Process Analytical Technology (PAT) Platform to Monitor Cell Cultures In-Line and in Real Time, from Process Development to Manufacturing
From process development to GMP clinical supply, process design, facility design and construction, tech transfer and training, and operational launch, your multidisciplinary team will work with you, delivering optimal results and guaranteeing your success.
Msynth®plus products for organic synthesis in quality-conscious or regulated industries are accompanied by qualification dossiers and the option to sign change control agreements.
Merck, today announced the opening of its advanced GMP bioproduction facility in Martillac, France, offering a full, single-use process train to speed a molecule's journey to the clinic.
Our state-of-the-art courses are designed to help biopharmaceutical manufacturers meet critical needs for process efficiency and current Good Manufacturing Practice compliance.