آمنیومکس یک محیط کامل برای کشت سلول های مایع آمنیوتیک انسانی برای مطالعات سیتوژنتیک و روش های تشخیصی آزمایشگاهی است. نمونههای مایع آمنیوتیک اولیه انسان به مدت شش روز در محیط کامل امنیومکس قبل از اندازهگیری تعداد کل کلنیها و تعداد کل کلنیهای میتوزی کشت داده میشوند. امنیومکس حاوی سرم جنین گاو (FBS)، جنتامایسین و ال-گلوتامین برای به حداکثر رساندن اتصال و رشد سلولی است. این محیط بهینه شده همچنین دارای یک سیستم بافرینگ پیشرفته است که ثبات pH بیشتری را در زمان کشت سلول ها فراهم می کند.
محصولات مرتبط
Product Overview
Gibco™ AmnioMAX™ - II Complete Medium is a fully-supplemented medium developed for the short term culture of human amniotic fluid cells for cytogenetic studies and in vitro diagnostic procedures
:Gibco™ AmnioMAX™ - II Complete Medium features
Ready-to-use format
Quality and performance testing
Unique, optimized formulation
Ready-to-use format
Gibco™ AmnioMAX™ - II Complete Medium is a frozen, 1X medium, ready to use upon thawing. No supplementation is required. Thawed medium can be stored at 2–8°C for up to ten days
Quality and performance testing
Every lot of Gibco™ AmnioMAX™ - II Complete Medium is performance tested by a certified US reference cytogenetics laboratory to ensure consistently superior performance. Pooled primary human amniotic fluid samples are cultured for six days in Gibco™ AmnioMAX™ - II Complete Medium before measuring the total number of colonies and total number of mitotic colonies. In addition, each lot is tested for pH and osmolality and must pass a sterility test prior to lot release
Unique, optimized formulation
Gibco™ AmnioMAX™ - II Complete Medium contains Fetal Bovine Serum (FBS), gentamicin, and L-glutamine to maximize cell attachment and growth. This optimized medium also has an enhanced buffering system that provides greater pH stability during culture manipulations
Product Use
For in vitro diagnostic use
cGMP Manufacturing and Quality System
Gibco™ AmnioMAX™ - II Complete Medium is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards
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