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LLC-MK2 Original
LLC-MK2 Original
规格:
货期:
编号:TS211636
品牌:Testobio
产品名称: LLC-MK2 Original
商品货号: TS211636
Organism: Macaca mulatta, monkey, rhesus
Tissue: kidney
Product Format: frozen
Morphology: epithelial
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: Normal
Age: adult
Storage Conditions: liquid nitrogen vapor phase
Images:
Genes Expressed:
plasminogen activator
Cellular Products:
plasminogen activator
Virus Susceptibility: Bovine viral diarrhea virus 1 , Bovine viral diarrhea virus 1
Human poliovirus 1
Human Coxsackievirus B4
Comments:
The serum used in the medium should be pre-tested for good quality.
Some lots of horse serum do support satisfactory growth.

Adaptation to other types of sera generally results in slow growth with a prolonged lag in growth.

Complete Growth Medium: Medium 199 (with 1.68 g/L bicarbonate), 99%; horse serum, 1%
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-0.53mMxa0 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 with 5 to 15 minutes).xa0Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach.xa0 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. To remove trypsin-EDTA solution, transfer cell suspension toxa0 centrifuge tube and spin atapproximatelyxa0125 x g for 5 to10 minutes.
  6. Discard supernatant and resuspend cells in fresh culture medium.xa0 Add appropriate aliquots of cell suspension to new culture vessels.xa0
  7. Place culture vessels in incubators at 37°C.

Subcultivation Ratio: A subcultivation ratio of 1:2 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: RN Hull
Deposited As: Macaca mulatta
References:

American Association of Anatomists. Sixty-ninth annual session; Marquette University School of Medicine, Milwaukee, Wisconsin. Anat. Rec. 124: 490, 1956.

Hull RN, et al. Growth characteristics of monkey kidney cell strains LLC-MK1, LLC-MK2, and LLC-MK2(NCTC-3196) and their utility in virus research. J. Exp. Med. 115: 903-918, 1962. PubMed: 14449901

Hull RN, Tritch OJ. Characterization of cell strains by viral susceptibility. Natl. Cancer Inst. Monogr. 7: 161-172, 1962. PubMed: 14449902

首页 > 产品中心 > 微生物培养 > 菌株 > null > LLC-MK2 Original

LLC-MK2 Original

  • 货号: TS211636
  • 好评
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  • 品牌 : TESTOBIO
产品名称: LLC-MK2 Original
商品货号: TS211636
Organism: Macaca mulatta, monkey, rhesus
Tissue: kidney
Product Format: frozen
Morphology: epithelial
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: Normal
Age: adult
Storage Conditions: liquid nitrogen vapor phase
Images:
Genes Expressed:
plasminogen activator
Cellular Products:
plasminogen activator
Virus Susceptibility: Bovine viral diarrhea virus 1 , Bovine viral diarrhea virus 1
Human poliovirus 1
Human Coxsackievirus B4
Comments:
The serum used in the medium should be pre-tested for good quality.
Some lots of horse serum do support satisfactory growth.

Adaptation to other types of sera generally results in slow growth with a prolonged lag in growth.

Complete Growth Medium: Medium 199 (with 1.68 g/L bicarbonate), 99%; horse serum, 1%
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-0.53mMxa0 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 with 5 to 15 minutes).xa0Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach.xa0 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. To remove trypsin-EDTA solution, transfer cell suspension toxa0 centrifuge tube and spin atapproximatelyxa0125 x g for 5 to10 minutes.
  6. Discard supernatant and resuspend cells in fresh culture medium.xa0 Add appropriate aliquots of cell suspension to new culture vessels.xa0
  7. Place culture vessels in incubators at 37°C.

Subcultivation Ratio: A subcultivation ratio of 1:2 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: RN Hull
Deposited As: Macaca mulatta
References:

American Association of Anatomists. Sixty-ninth annual session; Marquette University School of Medicine, Milwaukee, Wisconsin. Anat. Rec. 124: 490, 1956.

Hull RN, et al. Growth characteristics of monkey kidney cell strains LLC-MK1, LLC-MK2, and LLC-MK2(NCTC-3196) and their utility in virus research. J. Exp. Med. 115: 903-918, 1962. PubMed: 14449901

Hull RN, Tritch OJ. Characterization of cell strains by viral susceptibility. Natl. Cancer Inst. Monogr. 7: 161-172, 1962. PubMed: 14449902

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