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WISH
WISH
規格:
價格:
編號:B165953
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
WISH
商品貨號
B165953
Organism
Homo sapiens, human
Tissue
HeLa contaminant
培養基
Product Format
frozen
Morphology
epithelial
Culture Properties
adherent
Biosafety Level
2

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.

Storage Conditions
liquid nitrogen vapor phase
Derivation
This line was originally thought to be derived from normal amnion, but was subsequently found, based on isoenzyme analysis, HeLa marker chromosomes, and DNA fingerprinting, to have been established via HeLa cell contamination.
Antigen Expression
The cells are positive for keratin by immunoperoxidase staining.
HeLa Markers
Y
Genes Expressed
The cells are positive for keratin by immunoperoxidase staining.
The cells and tumors formed from the cells are positive for Dopa decarboxylase and are negative for the TAG-72 antigen.
Cellular Products
keratin
Virus Susceptibility
Human poliovirus 1
Human poliovirus 2
Human adenovirus 3
Vesicular stomatitis virus
Comments

NOTE: Cells of this line contain HeLa marker chromosomes, and were derived via HeLa contamination

 

Complete Growth Medium

EMEM (30-2003) supplemented with 10% FBS (30-2020)

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. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. 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 to 15 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.
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting. 
  5. Add appropriate aliquots of the cell suspension to new culture vessels. 
  6. Incubate cultures at 37°C.

Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:10 is recommended

Medium Renewal: Twice per week


Cryopreservation
culture medium 95%; DMSO, 5%
Culture Conditions
Temperature: 37°C
STR Profile
Amelogenin: X
CSF1PO: 9,10
D13S317: 13.3
D16S539: 9,10
D5S818: 11,12
D7S820: 8,12
THO1: 7
TPOX: 8,12
vWA: 16,18
Isoenzymes
G6PD, A
Name of Depositor
L Hayflick
Deposited As
Homo sapiens
References

Hayflick L. The establishment of a line (WISH) of human amnion cells in continuous cultivation. Exp. Cell Res. 23: 14-20, 1961. PubMed: 13712490

Buynak EB, et al. Infectivity Stability of Live Measles-Virus Vaccine. Am. J. Dis. Child. 103:460, 1962.

Hulkower KI, et al. Induction of prostaglandin H synthase-2 and tumor necrosis factor-alpha in human amnionic WISH cells by various stimuli occurs through distinct intracellular mechanisms. J. Pharmacol. Exp. Ther. 280: 1065-1074, 1997. PubMed: 9023325

Lundgren DW, et al. Hypotonic stress increases cyclooxygenase-2 expression and prostaglandin release from amnion-derived WISH cells. J. Biol. Chem. 272: 20118-20124, 1997. PubMed: 9242685

Perkins DJ, Kniss DA. Rapid and transient induction of cyclo-oxygenase 2 by epidermal growth factor in human amnion-derived WISH cells. Biochem. J. 321: 677-681, 1997. PubMed: 9032453

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