你好,请登录   免费注册    |    收藏本站
联系电话: 0574-87917803
联系电话: call_new 0574-87917803
Panc 02.13
Panc 02.13
规格:
货期:
编号:TS211131
品牌:Testobio
产品名称: Panc 02.13
商品货号: TS211131
Organism: Homo sapiens, human
Tissue: pancreas
Cell Type: Epithelial
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: 64 years
Gender: female
Ethnicity: White
Derivation:
Panc 02.13 is a pancreatic adenocarcinoma epithelial cell line derived in 1995 from a primary tumor removed from the head-of-the-pancreas of a female with pancreatic adenocarcinoma.
Clinical Data:
female
64 years
White
Antigen Expression:
MHC class I +; MHC class II -
Blood type A; Rh+
Oncogene: K-ras + (wild-type) RefJaffee EM, et al. Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J. Sci. Am. 4: 194-203, 1998. PubMed: 9612602
Genes Expressed:
cytokeratins 7 and 18
Cellular Products:
cytokeratins 7 and 18
Tumorigenic: Yes
Effects:
Yes, forms tumors in nude or SCID mice
Comments:
The cells have a reported plating efficiency of 100%.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium:
  • 10 Units/ml human recombinant insulin
  • fetal bovine serum to a final concentration of 15%

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-0.03% (w/v) 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

Subculture Ratio: 1:3 to 1:4
Medium Renewal: Every 2 to 3 days.
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%
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 12
D13S317: 8,11
D16S539: 9,12
D5S818: 12
D7S820: 7,11
THO1: 6,9.3
TPOX: 8
vWA: 16,18
Population Doubling Time: 33.9 hrs
Name of Depositor: EM Jaffee
Deposited As: human
Year of Origin: 1995
References:

Jaffee EM, et al. Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J. Sci. Am. 4: 194-203, 1998. PubMed: 9612602

Jaffee EM, et al. Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J. Sci. Am. 4: 194-203, 1998. PubMed: 9612602

首页 > 产品中心 > 微生物培养 > 菌株 > null > Panc 02.13

Panc 02.13

  • 货号: TS211131
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: Panc 02.13
商品货号: TS211131
Organism: Homo sapiens, human
Tissue: pancreas
Cell Type: Epithelial
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: 64 years
Gender: female
Ethnicity: White
Derivation:
Panc 02.13 is a pancreatic adenocarcinoma epithelial cell line derived in 1995 from a primary tumor removed from the head-of-the-pancreas of a female with pancreatic adenocarcinoma.
Clinical Data:
female
64 years
White
Antigen Expression:
MHC class I +; MHC class II -
Blood type A; Rh+
Oncogene: K-ras + (wild-type) RefJaffee EM, et al. Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J. Sci. Am. 4: 194-203, 1998. PubMed: 9612602
Genes Expressed:
cytokeratins 7 and 18
Cellular Products:
cytokeratins 7 and 18
Tumorigenic: Yes
Effects:
Yes, forms tumors in nude or SCID mice
Comments:
The cells have a reported plating efficiency of 100%.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium:
  • 10 Units/ml human recombinant insulin
  • fetal bovine serum to a final concentration of 15%

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-0.03% (w/v) 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

Subculture Ratio: 1:3 to 1:4
Medium Renewal: Every 2 to 3 days.
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%
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 12
D13S317: 8,11
D16S539: 9,12
D5S818: 12
D7S820: 7,11
THO1: 6,9.3
TPOX: 8
vWA: 16,18
Population Doubling Time: 33.9 hrs
Name of Depositor: EM Jaffee
Deposited As: human
Year of Origin: 1995
References:

Jaffee EM, et al. Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J. Sci. Am. 4: 194-203, 1998. PubMed: 9612602

Jaffee EM, et al. Development and characterization of a cytokine-secreting pancreatic adenocarcinoma vaccine from primary tumors for use in clinical trials. Cancer J. Sci. Am. 4: 194-203, 1998. PubMed: 9612602

合作单位: