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OptiPRO™ SFM
  • 品牌:OptiPRO
  • 发布日期: 2019-09-26
  • 更新日期: 2025-07-26
产品详请
产地
品牌 OptiPRO
货号 12309-050
用途
英文名称
包装规格 100 ml
纯度 %
CAS编号
保质期 6个月
是否进口

货号: 12309-050

规格

Form:  Liquid

Format:  Bottle(s)

Cell Line:  HeLa, MDBK, MDCK, PK-15, BHK-21, COS-7, VERO

Glutamine:  No Glutamine

Serum Level:  Serum-Free

Supplements:  Hypoxanthine, Thymidine

Concentrated:   1 X

Culture Type:   Cell Culture

Product Size:   100 mL

Classification:   Animal Origin-Free, Serum-Free, Low-Protein

Endotoxin Level:   Low

Volume (Metric): 100 ml

Included Antibiotics: No Antibiotics

Phenol Red Indicator:       Phenol Red

Sodium Pyruvate Additive:     Sodium Pyruvate

Sodium Bicarbonate Buffer:    Sodium Bicarbonate

Shipping Condition:   Room Temperature

内容及储存

Storage conditions: 2 – 8°C. Protect fromlight.

Shipping conditions: Ambient

Shelf life: 24 months from date of  manufacture

描述

OptiPRO™ SFM is a serum-free, animal origin-free culture medium designed for growth of several kidney-derived cell lines including MDBK, MDCK, PK-15 and VERO for virus or recombinant protein production. In addition, OptiPRO™ SFM has successfully grown other cell lines, such as Hela, BHK-21 and COS-7. Gibco® OptiPRO™ SFM features:
? Serum-free, animal origin-free, low protein formulation
? Direct adaptation for many popular cell lines

Serum-free, animal origin-free, low protein formulation
Gibco® OptiPRO™ SFM is formulated with a very low protein concentration (< 10 μg/ml), allowing for easier purification of your recombinant protein.

Direct adaptation for many popular cell lines
Gibco® OptiPRO™ SFM has been designed for growth of kidney-derived cell lines such as MDCK, MDBK, VERO and PK-15. In addition, OptiPRO™ SFM has successfully grown other cell lines, such as Hela, BHK-21 and COS-7, allowing you to choose a single medium for multiple cell lines.
Product Use
For Research Use Only. Not for use in diagnostic procedures.


cGMP Manufacturing and Quality System
Gibco® OptiPRO™ SFM 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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