QM7 (Quail muscle clone 7) 智立中特生物

详情描述：

M7 (Quail Muscle Clone 7)
平台编号: zl-057855
规格: frozen
细胞信息: QM7 (Quail muscle clone 7)
数量：大量
生长状态：贴壁生长
ATCC Number：CRL-1962?
相关疾病：纤维肉瘤
年限：1 to 3 weeks
细胞形态：成纤维样
运输方式：冻存运输
细胞类型：其他细胞类型
是否是肿瘤细胞：0
物种来源：其他
组织来源：muscle
规格：1mg Designations: QM7 (Quail muscle clone 7)
Depositors: ?PB Antin
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
Organism: Coturnix coturnix japonica
Morphology:fibroblast


Source: Tissue: muscle
Disease: fibrosarcoma
Cell Type: myoblast myoblast; chemically induced
Cellular Products:desmin; cardiac troponin T; cardiac troponin C; skeletal troponin T; skeletal troponin I; alpha tropomyosin; muscle creatine kinase; myosin light chain 2; myosin heavy chain (ventricular form)
Permits/Forms:In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
Age: 1 to 3 weeks
Comments:The QM7 cell line was derived from the QT6 fibrosarcoma originally isolated by Moscovici, et al. from a tumor that developed in a bird treated with methylcholanthrene.
QM7 is a serum inducible myogenic cell line.
The cells replicate as myoblasts in medium containing serum.
When switched to medium without serum, the cells cease dividing and fuse to form large multinucleated myotubes.
In the myotube state, the cells express muscle specific proteins such as desmin, cardiac troponin T, cardiac troponin C, skeletal troponin T, skeletal troponin I, alpha tropomyosin.
Mucle creatine kinase, myosin light chain 2 and a ventricular form of myosin heavy chain.
They do not express any known form of alpha actin.
QM7 cells transfect with high efficiency, and are useful for studying many aspects of muscle differentiation and gene expression.
The myoblastic population will become depleted rapidly if the cultures are allowed to become confluent.
To prevent loss of myoblastic cell, cultures should be subcultured before they become confluent and the line should be recloned periodically with selection for myoblastic cells.
Propagation: ATCC complete growth medium: Medium 199 with Earle's BSS, 80%; tryptose phosphate broth, 10%; fetal bovine serum, 10%
Temperature: 37.0?C
Subculturing: Protocol: The myoblastic population will become depleted rapidly if the cultures are allowed to become confluent. Remove spent medium, add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin solution. Incubate the flask at room temperature until the cells detach (about 5 minutes). Add fresh medium, aspirate and dispense into new flasks.
Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:5 is recommended
Medium Renewal: Every 2 to 3 days
References: 23002: Antin PB, Ordahl CP. Isolation and characterization of an avian myogenic cell line. Dev. Biol. 143: 111-121, 1991. PubMed: 1985013
70419: Rong S, Sheppard MG. Processes for preparation of Marek's disease virus using continuous avian cell lines. US Patent 6,410,297 dated Jun 25 2002