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AMNIOMAX C100, COMBO EACH,12558011,Invitrogen

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订货号 6MX6853
品牌型号 Invitrogen 12558011
货期 询货期
最小订货量 1套
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产品介绍 Product Description
规格
Included Antibiotics: Gentamicin
Product Line: AmnioMAX™
Serum Level: Standard Serum
Species: Human
Form: Liquid
Cell Type: Amniocytes
储存
Basal Medium (90 ml):
Storage: 2 – 8°C
Ships: Ambient temperature
Shelf life: 16 months from date of manufacture

Supplement (15 ml):
Storage: -5 to -20°C
Ships: Frozen
Shelf life: 16 months from date of manufacture

Use complete medium within 7–10 days once opened.
描述

Gibco® AmnioMAX™ C-100 Complete Medium is a kit used to prepare 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™ C-100 Complete Medium features:

• Easy-to-use format
• Quality and performance testing
• Unique, optimized formulation

Easy-to-use format
Gibco® AmnioMAX™ C-100 Complete Medium is a two-part kit for preparation of a complete medium that requires no additional supplementation. The complete medium can be stored at 2–8°C for up to ten days.

Quality and performance testing
Every lot of Gibco® AmnioMAX™ C-100 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™ C-100 Complete Medium before measuring the total number of colonies and total number of mitotic colonies. In addition, each lot is tested for sterility, pH and osmolality.

Unique, optimized formulation
Gibco® AmnioMAX™ C-100 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™ C-100 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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