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2H-11
2H-11
规格:
货期:
编号:TS212934
品牌:Testobio
产品名称: 2H-11
商品货号: TS212934
Organism: Mus musculus, mouse
Tissue: axillary lymph node/vascular epithelium
Cell Type: endothelial, SV40 transformed
Product Format: frozen
Morphology: epithelial
Culture Properties: adherent
Biosafety Level: 2 Cells contain polyomavirus 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.

Age: adult
Gender: Male
Strain: C3H/HeJ
Storage Conditions: liquid nitrogen vapor phase
Derivation:
The 2H-11 cell line was derived from a solid tumor in nude mice injected with SVEC4-10EHR1 (see ATCC CRL-2161).
The line was cloned in 1992 by limiting dilution.
Clinical Data:
male
Antigen Expression:
H-2 K; VCAM
Tumorigenic: Yes
Effects:
Yes, the cells induce spindle tumors with some of the histopathologic characteristics of human Kaposi Sarcoma after a latency period of approximately 14 weeks
Comments:

The cells are sensitive to lysis by activated macrophages as measured in the chromium release assay.

This clone retains the ability to differentiate on a synthetic basement-like membrane.

The cells express the cell surface major histocompatibility complex class I antigen, H-2 k, of the parental cell line, and express VCAM (vascular cell adhesion molecule).

The cells stain positively for SV40 T antigen.

Complete Growth Medium:

The base medium for this cell line is Dulbeccos Modified Eagles Medium (DMEM; ATCC 30-2002). To make the complete medium add heat-inactivated Fetal Bovine Serum (FBS; ATCC 30-2020) to a final concentration of 10%.

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 mMxa0EDTA 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: 1:4 to 1:6
Medium Renewal: 2 to 3 times a week.
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%
Name of Depositor: KA OConnell
References:

OConnell KA, Edidin M. A mouse lymphoid endothelial cell line immortalized by simian virus 40 binds lymphocytes and retains functional characteristics of normal endothelial cells. J. Immunol. 144: 521-525, 1990. PubMed: 2153170

OConnell KA, Rudmann AA. Cloned spindle and epithelioid cells from murine Kaposis sarcoma-like tumors are of endothelial origin. J. Invest. Dermatol. 100: 742-745, 1993. PubMed: 8496612

OConnell K, et al. Endothelial cells transformed by SV40 T antigen cause Kaposis sarcomalike tumors in nude mice. Am. J. Pathol. 139: 743-749, 1991. PubMed: 1928299

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2H-11

  • 货号: TS212934
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  • 品牌 : TESTOBIO
产品名称: 2H-11
商品货号: TS212934
Organism: Mus musculus, mouse
Tissue: axillary lymph node/vascular epithelium
Cell Type: endothelial, SV40 transformed
Product Format: frozen
Morphology: epithelial
Culture Properties: adherent
Biosafety Level: 2 Cells contain polyomavirus 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.

Age: adult
Gender: Male
Strain: C3H/HeJ
Storage Conditions: liquid nitrogen vapor phase
Derivation:
The 2H-11 cell line was derived from a solid tumor in nude mice injected with SVEC4-10EHR1 (see ATCC CRL-2161).
The line was cloned in 1992 by limiting dilution.
Clinical Data:
male
Antigen Expression:
H-2 K; VCAM
Tumorigenic: Yes
Effects:
Yes, the cells induce spindle tumors with some of the histopathologic characteristics of human Kaposi Sarcoma after a latency period of approximately 14 weeks
Comments:

The cells are sensitive to lysis by activated macrophages as measured in the chromium release assay.

This clone retains the ability to differentiate on a synthetic basement-like membrane.

The cells express the cell surface major histocompatibility complex class I antigen, H-2 k, of the parental cell line, and express VCAM (vascular cell adhesion molecule).

The cells stain positively for SV40 T antigen.

Complete Growth Medium:

The base medium for this cell line is Dulbeccos Modified Eagles Medium (DMEM; ATCC 30-2002). To make the complete medium add heat-inactivated Fetal Bovine Serum (FBS; ATCC 30-2020) to a final concentration of 10%.

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 mMxa0EDTA 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: 1:4 to 1:6
Medium Renewal: 2 to 3 times a week.
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%
Name of Depositor: KA OConnell
References:

OConnell KA, Edidin M. A mouse lymphoid endothelial cell line immortalized by simian virus 40 binds lymphocytes and retains functional characteristics of normal endothelial cells. J. Immunol. 144: 521-525, 1990. PubMed: 2153170

OConnell KA, Rudmann AA. Cloned spindle and epithelioid cells from murine Kaposis sarcoma-like tumors are of endothelial origin. J. Invest. Dermatol. 100: 742-745, 1993. PubMed: 8496612

OConnell K, et al. Endothelial cells transformed by SV40 T antigen cause Kaposis sarcomalike tumors in nude mice. Am. J. Pathol. 139: 743-749, 1991. PubMed: 1928299

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