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L8
L8
規格:
價格:
編號:B164950
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱
L8
商品貨號
B164950
Organism
Rattus norvegicus, rat
Tissue
skeletal muscle
培養基
Cell Type
myoblast
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.

Disease
Carcinogen
Age
newborn
Applications
transfection host
Storage Conditions
liquid nitrogen vapor phase
Derivation
This line was originally isolated by D. Yaffe in 1969 from primary rat skeletal muscle cultures.

Unlike the L6 cell line (ATCC CRL-1458) no carcinogen was used to establish the L8 line.

Genes Expressed
creatine phosphokinase (CPK); myosin
Cellular Products
creatine phosphokinase (CPK); myosin
Comments

Upon becoming confluent, L8 will fuse to form cross striated multinucleated muscle fibers.

It is recommended that early passages be preserved in liquid nitrogen and that the line be recloned periodically and reselected for progeny that have the ability to fuse.

It is important that the cells be subcultured when the flask is about 60% confluent. The myoblastic population will be depleted if the cultures are allowed to become confluent since most of the cells will fuse into nondividing syncytia. To avoid this, one must subculture before before the cultures become confluent and should reclone periodically and select myoblastic clones.

Complete Growth Medium
A 4:1 mixture of Dulbecco's modified Eagle's medium and Medium 199, 89%; chicken embryo extract (US Biological cat# C3999), 1%; horse serum, 10%
Subculturing
Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Add 2.0 to 3.0 mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 minutes).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
  3. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  4. Add appropriate aliquots of the cell suspension to new culture vessels at a density of 2000 cells/sq. cm.
  5. Incubate cultures at 37°C.
Subcultivation Ratio: An inoculation density of 4000 viable cells per cm2 of flask or dish surface area is recommended.
Medium Renewal: Twice per week

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.
Cryopreservation
Culture medium, 95%; DMSO, 5%
Name of Depositor
B Paterson
Deposited As
Rattus sp.
Passage History
It is recommended that early passages be preserved in liquid nitrogen and that the line be recloned periodically and reselected for progeny that have the ability to fuse.
References

Richler C, Yaffe D. The in vitro cultivation and differentiation capacities of myogenic cell lines. Dev. Biol. 23: 1-22, 1970. PubMed: 5481965

Yaffe D, Saxel O. A myogenic cell line with altered serum requirements for differentiation. Differentiation 7: 159-166, 1977. PubMed: 558123

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