| 產(chǎn)品名稱 | IC-21 |
|---|---|
| 商品貨號 | B164823 |
| Organism | Mus musculus, mouse |
| Cell Type | peritoneal macrophage; SV40 transformed |
| Product Format | frozen |
| 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. |
| Strain | C57BL/6 |
| Applications | Biological response Ref
  Singer JA, et al. Interaction of a mouse macrophage cell line with homologous erythrocytes. J. Reticuloendothel. Soc. 31: 489-499, 1982. PubMed: 7120230 transfection host |
| Derivation | The IC-21 cell line was derived by transformation of normal C57BL/6 mouse peritoneal macrophages with SV40. |
| Receptor Expression | Receptor expression: Fc Ref |
| Genes Expressed | lysozyme |
| Cellular Products | lysozyme |
| Comments | This line shares many properties with normal mouse macrophages and display macrophage specific antigens.
They have phagocytic and cytolytic properties, can lyse tumor targets in vitro and appear to be more differentiated than cells of the P388D1 macrophage line.
Trypsin is toxic to this line.
The cells produce large quantities of acid and the medium should be changed frequently.
Tested and found negative for ectromelia virus (mousepox). |
| Complete Growth Medium | The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, ATCC 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (ATCC 30-2020) to a final concentration of 10%.
|
| Subculturing | Rinse the monolayer twice with 10 to 15 mL of Ca++/Mg++-free PBS (ATCC® No. 30-2200), then add an additional 10 to 15 mL of the same solution to the cells. Let the culture stand for 5 to 10 minutes at room temperature, then gently bang or tap the flask, or use a sterile cell scraper to dislodge any adherent cells. Pipette the detached cells up and down using a 5 or 10 ml sterile pipette to break up the clumps but avoid the creation of foam. Centrifuge the cells at 125 x g for 5 to 7 minutes and aspirate the supernatant. Gently resuspend the cells in complete growth medium and perform a cell count to calculate the total viable cell number. Subculture the cells into new vessels using a split ratio of 1:2 to 1:4.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
Medium Renewal: 3 times per week |
| Cryopreservation | culture medium 95%; DMSO, 5% |
| Culture Conditions | Temperature: 37.0°C Atmosphere: air, 95%; carbon dioxide (CO2), 5% |
| Name of Depositor | WS Walker |
| Deposited As | Mus musculus |
| References | Walker WS. Separate Fc-receptors for immunoglobulins IgG2a and IgG2b on an established cell line of mouse macrophages. J. Immunol. 116: 911-914, 1976. PubMed: 1254971 Walker WS, Gandour DM. Detection and functional assessment of complement receptors on two murine macrophage-like cell lines. Exp. Cell Res. 129: 15-21, 1980. PubMed: 7428810 Walker WS. Mediation of macrophage cytolytic and phagocytic activities by antibodies of different classes and class-specific Fc-receptors. J. Immunol. 119: 367-373, 1977. PubMed: 886183 Mocarelli P, et al. A permanent line of macrophages with normal activity in a primary antibody response in vitro. Immunol. Commun. 2: 441-447, 1973. PubMed: 4357034 Mauel J, Defendi V. Infection and transformation of mouse peritoneal macrophages by simian virus 40. J. Exp. Med. 134: 335-350, 1971. PubMed: 4326994 Holden HT, et al. . Fed. Proc. 38: 1093 (abstract 4582), 1979. Walker WS, Demus A. Antibody-dependent cytolysis of chicken erythrocytes by an in vitro- established line of mouse peritoneal macrophages. J. Immunol. 114: 765-769, 1975. PubMed: 1167563 Singer JA, et al. Interaction of a mouse macrophage cell line with homologous erythrocytes. J. Reticuloendothel. Soc. 31: 489-499, 1982. PubMed: 7120230 Takao S, et al. Role of reactive oxygen metabolites in murine peritoneal macrophage phagocytosis and phagocytic killing. Am. J. Physiol. 271: C1278-C1284, 1996. PubMed: 8897835 Serio C, et al. Macrophage functional heterogeneity: evidence for different antibody-dependent effector cell activities and expression of Fc-receptors among macrophage subpopulations. J. Reticuloendothel. Soc. 25: 197-206, 1979. PubMed: 439098 Standard Practice for Testing for Biological Responses to Particles in Vitro. West Conshohocken, PA:ASTM International;ASTM Standard Test Method F 1903-98R03. |
| 梅經(jīng)理 | 17280875617 | 1438578920 |
| 胡經(jīng)理 | 13345964880 | 2438244627 |
| 周經(jīng)理 | 17757487661 | 1296385441 |
| 于經(jīng)理 | 18067160830 | 2088210172 |
| 沈經(jīng)理 | 19548299266 | 2662369050 |
| 李經(jīng)理 | 13626845108 | 972239479 |
