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7F2
7F2
規(guī)格:
貨期:
編號:B163830
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 7F2
商品貨號 B163830
Organism Mus musculus, mouse
Tissue bone marrow
Cell Type osteoblast
Product Format frozen
Morphology fibroblast
Culture Properties adherent
Biosafety Level 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Age 5 to 6 weeks
Gender male
Storage Conditions liquid nitrogen vapor phase
Disclosure This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC.
Images
Derivation
7F2 is a spontaneously immortalized cell line isolated from p53-/- mouse bone marrow taken from the femur and subsequently cloned. (Moore EE. Preparation of immortalized cells. US Patent 5,830,682 dated Nov 3 1998)
Clinical Data
male
Genes Expressed
alkaline phosphatase
Comments

The cells appeared to correspond to mature osteoblasts because they express alkaline phosphatase, secrete type I collagen, show a significant cyclic adenosine monophosphate response to parathyroid hormone, secrete osteocalcin, and mineralize extensively. However, in contrast to mature osteoblasts, this clone can be induced to undergo massive adipocyte differentiation, and this differentiation is accompanied by the complete loss of expression of all osteoblastic markers except alkaline phosphatase. These observations indicate that some cells that have acquired all of the characteristics of mature osteoblasts can be diverted to the adipocyte pathway. RefThompson DL, et al. The derivation and characterization of stromal cell lines from the bone marrow of p53-/- mice: new insights into osteoblast and adipocyte differentiation. J. Bone Miner. Res. 13: 195-204, 1998. PubMed: 9495512

Complete Growth Medium Alpha minimum essential medium with 2 mM l-glutamine and 1 mM sodium pyruvate without ribonucleosides and deoxyribonucleosides, 90%; fetal bovine serum, 10%
Subculturing
Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37°C) until the cells detach.
Centrifuge the cell suspension at 1000 rpm for 10 minutes, resuspend the pellet in fresh medium, aspirate and dispense into new flasks.
Subculture before the cells become confluent.
Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:10 is recommended
Medium Renewal: Every 2 to 3 days
Cryopreservation
culture medium 95%; DMSO, 5%
Culture Conditions
Temperature: 37°C
Name of Depositor ZymoGenetics, Inc.
Deposited As mouse
U.S. Patent Number
References

Moore EE. Preparation of immortalized cells. US Patent 5,830,682 dated Nov 3 1998

Thompson DL, et al. The derivation and characterization of stromal cell lines from the bone marrow of p53-/- mice: new insights into osteoblast and adipocyte differentiation. J. Bone Miner. Res. 13: 195-204, 1998. PubMed: 9495512

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