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PA317 LXSN
PA317 LXSN
规格:
货期:
编号:TS211139
品牌:Testobio
产品名称: PA317 LXSN
商品货号: TS211139
Organism: Mus musculus, mouse
Tissue: embryo
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
Biosafety Level: 2 Cells contain human papilloma viral DNA sequences

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: Leukemia
Age: embryo
Strain: NIH/Swiss
Applications:
Virions produced from the transfected Psi-2 cells were used to infect the amphotropic packaging line PA317, and infected cells were selected in medium containing G418.
PA317 LXSN cells produce an amphoteric retrovirus with an empty neo control vector, 5 long terminal repeat (LTR) from the Moloney murine leukemia virus (MoMuLV) multiple cloning region and 3 LTR from MoMuLV.
The vector also contains a gene controlling resistance to neomycin transcribed from the SV40 promoter.
This line is useful as a negative control for the use of PA317 LXSN 16E6E7 (see ATCC CRL-2203).
Derivation:
PA317 LXSN is a packaging cell line developed by transfection of the retrovirus vector pLXSN into the Psi-2 ecotropic packaging cell line.
Virions produced from the transfected Psi-2 cells were used to infect the amphotropic packaging line PA317, and infected cells were selected in medium containing G418.
Comments:
PA317 LXSN is a packaging cell line developed by transfection of the retrovirus vector pLXSN into the Psi-2 ecotropic packaging cell line.
Virions produced from the transfected Psi-2 cells were used to infect the amphotropic packaging line PA317, and infected cells were selected in medium containing G418.
PA317 LXSN cells produce an amphoteric retrovirus with an empty neo control vector, 5 long terminal repeat (LTR) from the Moloney murine leukemia virus (MoMuLV) multiple cloning region and 3 LTR from MoMuLV.
The vector also contains a gene controlling resistance to neomycin transcribed from the SV40 promoter.
This line is useful as a negative control for the use of PA317 LXSN 16E6E7 (see ATCC CRL-2203).
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing:
Subcultivation Ratio: A subcultivation ratio of 1:6 to 1:12 is recommended
Medium Renewal: Every 2 to 3 days
Remove medium, rinse flask with fresh 0.25% trypsin, 0.02% EDTA and remove trypsin, Add an additional 1 to 2 ml of trypsin solution, and allow the flask to sit at room temperature (or 37C) until the cells detach.
Add fresh medium, aspirate and dispense into new flasks.
Cryopreservation:
Culture medium, 95%; DMSO, 5%
Name of Depositor: DA Galloway
Deposited As: Mus musculus
References:

Halbert CL, et al. The E7 gene of human papillomavirus type 16 is sufficient for immortalization of human epithelial cells. J. Virol. 65: 473-478, 1991. PubMed: 1845902

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PA317 LXSN

  • 货号: TS211139
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  • 品牌 : TESTOBIO
产品名称: PA317 LXSN
商品货号: TS211139
Organism: Mus musculus, mouse
Tissue: embryo
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
Biosafety Level: 2 Cells contain human papilloma viral DNA sequences

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: Leukemia
Age: embryo
Strain: NIH/Swiss
Applications:
Virions produced from the transfected Psi-2 cells were used to infect the amphotropic packaging line PA317, and infected cells were selected in medium containing G418.
PA317 LXSN cells produce an amphoteric retrovirus with an empty neo control vector, 5 long terminal repeat (LTR) from the Moloney murine leukemia virus (MoMuLV) multiple cloning region and 3 LTR from MoMuLV.
The vector also contains a gene controlling resistance to neomycin transcribed from the SV40 promoter.
This line is useful as a negative control for the use of PA317 LXSN 16E6E7 (see ATCC CRL-2203).
Derivation:
PA317 LXSN is a packaging cell line developed by transfection of the retrovirus vector pLXSN into the Psi-2 ecotropic packaging cell line.
Virions produced from the transfected Psi-2 cells were used to infect the amphotropic packaging line PA317, and infected cells were selected in medium containing G418.
Comments:
PA317 LXSN is a packaging cell line developed by transfection of the retrovirus vector pLXSN into the Psi-2 ecotropic packaging cell line.
Virions produced from the transfected Psi-2 cells were used to infect the amphotropic packaging line PA317, and infected cells were selected in medium containing G418.
PA317 LXSN cells produce an amphoteric retrovirus with an empty neo control vector, 5 long terminal repeat (LTR) from the Moloney murine leukemia virus (MoMuLV) multiple cloning region and 3 LTR from MoMuLV.
The vector also contains a gene controlling resistance to neomycin transcribed from the SV40 promoter.
This line is useful as a negative control for the use of PA317 LXSN 16E6E7 (see ATCC CRL-2203).
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing:
Subcultivation Ratio: A subcultivation ratio of 1:6 to 1:12 is recommended
Medium Renewal: Every 2 to 3 days
Remove medium, rinse flask with fresh 0.25% trypsin, 0.02% EDTA and remove trypsin, Add an additional 1 to 2 ml of trypsin solution, and allow the flask to sit at room temperature (or 37C) until the cells detach.
Add fresh medium, aspirate and dispense into new flasks.
Cryopreservation:
Culture medium, 95%; DMSO, 5%
Name of Depositor: DA Galloway
Deposited As: Mus musculus
References:

Halbert CL, et al. The E7 gene of human papillomavirus type 16 is sufficient for immortalization of human epithelial cells. J. Virol. 65: 473-478, 1991. PubMed: 1845902

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