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SW 1990 [SW-1990, SW1990]
SW 1990 [SW-1990, SW1990]
规格:
货期:
编号:TS210835
品牌:Testobio
产品名称: SW 1990 SW-1990, SW1990
商品货号: TS210835
Organism: Homo sapiens, human
Tissue: pancreas; Derived from metastatic site:xa0spleen
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: adenocarcinoma
Age: 56 years
Gender: Male
Ethnicity: Caucasian
Storage Conditions: liquid nitrogen vapor phase
Karyotype: near triploid; range = 67 to 75
Images:
Derivation:
The SW 1990 line was established in 1978 from a spleen metastasis of a grade II pancreatic adenocarcinoma derived from the exocrine pancreas.

Clinical Data:
56 years
Caucasian
male
Antigen Expression:
Blood Type A; Rh +
Tumorigenic: Yes
Effects:
Yes, forms tumors in nude mice
Comments:
The cells have a reported plating efficiency of 29%.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Leibovitzs L-15 Medium, Catalog No. 30-2008. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

(Note: The L-15 medium formulation was devised for use in a free gas exchange with atmospheric air. A CO2 and air mixture is detrimental to cells when using this medium for cultivation)


Subculturing:

  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 that 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:xa0A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal:xa02 to 3 times per week


Cryopreservation:
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Temperature: 37°C
Atmosphere: air, 100%
STR Profile:
D5S818: 12, 13
D13S317: 8, 12
D7S820: 9, 10
D16S539: 13
vWA: 17
THO1: 9.3
Amelogenin: X
TPOX: 8, 9
CSF1PO: 10, 12

Population Doubling Time: 64 hrs
Name of Depositor: W McCombs
Deposited As: Homo sapiens
Year of Origin: 1978
References:

Kyriazis AP, et al. Establishment and characterization of human pancreatic adenocarcinoma cell line SW-1990 in tissue culture and the nude mouse. Cancer Res. 43: 4393-4401, 1983. PubMed: 6871872

首页 > 产品中心 > 微生物培养 > 菌株 > null > SW 1990 [SW-1990, SW1990]

SW 1990 [SW-1990, SW1990]

  • 货号: TS210835
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: SW 1990 SW-1990, SW1990
商品货号: TS210835
Organism: Homo sapiens, human
Tissue: pancreas; Derived from metastatic site:xa0spleen
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: adenocarcinoma
Age: 56 years
Gender: Male
Ethnicity: Caucasian
Storage Conditions: liquid nitrogen vapor phase
Karyotype: near triploid; range = 67 to 75
Images:
Derivation:
The SW 1990 line was established in 1978 from a spleen metastasis of a grade II pancreatic adenocarcinoma derived from the exocrine pancreas.

Clinical Data:
56 years
Caucasian
male
Antigen Expression:
Blood Type A; Rh +
Tumorigenic: Yes
Effects:
Yes, forms tumors in nude mice
Comments:
The cells have a reported plating efficiency of 29%.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Leibovitzs L-15 Medium, Catalog No. 30-2008. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

(Note: The L-15 medium formulation was devised for use in a free gas exchange with atmospheric air. A CO2 and air mixture is detrimental to cells when using this medium for cultivation)


Subculturing:

  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 that 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:xa0A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal:xa02 to 3 times per week


Cryopreservation:
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Temperature: 37°C
Atmosphere: air, 100%
STR Profile:
D5S818: 12, 13
D13S317: 8, 12
D7S820: 9, 10
D16S539: 13
vWA: 17
THO1: 9.3
Amelogenin: X
TPOX: 8, 9
CSF1PO: 10, 12

Population Doubling Time: 64 hrs
Name of Depositor: W McCombs
Deposited As: Homo sapiens
Year of Origin: 1978
References:

Kyriazis AP, et al. Establishment and characterization of human pancreatic adenocarcinoma cell line SW-1990 in tissue culture and the nude mouse. Cancer Res. 43: 4393-4401, 1983. PubMed: 6871872

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