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化工儀器網>產品展廳>試劑標物>行業專用試劑>生物試劑>25300-054 Trypsin-EDTA (0.05%), phenol red 胰酶

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25300-054 Trypsin-EDTA (0.05%), phenol red 胰酶

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重慶市華雅干細胞技術有限公司是中國中西部地區*家專業從事生物技術產品銷售(包括:生物試劑、生物耗材、儀器設備、技術產品等)、干細胞儲存、干細胞相關基礎研究、干細胞臨床應用研究及技術服務的新技術企業。供應造血干細胞培養基,神經干細胞培養基,干細胞無血清培養基,胚胎/IPS干細胞無血清培養基,心肌細胞分化培養基,外周血核型分析培養基。公司立足西南,面向全國,以“積極借鑒成功經驗,追求創新”為核心思想,將為客戶提供水平的干細胞產品和服務。

“華雅干細胞”是由我們公司的全體員工用心打造的一塊金質招牌,我們的團隊:富有激情、相互信任、目標*、熱愛干細胞事業、用心為我們的干細胞客戶服務。干細胞產業的蓬勃發展需要產業鏈中的每個成員精耕細作,協同發展,實踐創新。

華雅干細胞公司立志為中國干細胞產業的進步與發展做出應有的貢獻,為人類健康事業更上一層樓而不懈努力!


干細胞研究 干細胞治療產品 生物試劑 實驗耗材 藥物研發

描述

Gibco® Trypsin-EDTA is made from trypsin powder, an irradiated mixture of proteases derived from porcine pancreas. Due to its digestive strength, trypsin is widely used for cell dissociation, routine cell culture passaging, and primary tissue dissociation. The trypsin concentration required for dissociation varies with cell type and experimental requirements. See the complete range of Gibco® trypsin solutions and recommended dissociation conditions.

We offer a variety of trypsin formulations and animal origin-free TrypLE™ reagent that feature:

• Quality testing
• Documented traceability
• Dual-site cGMP Manufacturing
 

This trypsin solution is modified as follows:

With
• EDTA
• Phenol Red


The complete formulation is available.

Quality testing
Gibco® Trypsin solutions are tested for pH, osmolality, sterility, and performance. In addition, prior to manufacturing, the raw materials are verified for e-beam irradiation and tested for endotoxin, PPV, PCV 1/2, mycoplasma, bacterial, fungal, and viral contamination, as well as multiple activity assays, ash analysis, and moisture analysis.

Documented traceability
We can provide detailed documentation to meet your regulatory needs. Gibco® Trypsin information available includes lot traceability, animal origin certificates, lot analyses, irradiation certificates, a viral inactivation summary, and supply chain transparency.

cGMP manufacturing and quality system
Gibco® Trypsin 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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