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            當(dāng)前位置:上海復(fù)祥生物科技有限公司>>細(xì)胞庫>>小鼠腫瘤細(xì)胞、癌細(xì)胞>>CRL-2586EOMA 小鼠血管內(nèi)皮瘤細(xì)胞

            EOMA 小鼠血管內(nèi)皮瘤細(xì)胞

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            具體成交價以合同協(xié)議為準(zhǔn)

            產(chǎn)品型號:CRL-2586

            品       牌:ATCC

            廠商性質(zhì):生產(chǎn)商

            所  在  地:上海市

            更新時間:2024-11-14 20:42:35瀏覽次數(shù):2235

            聯(lián)系我時,請告知來自 化工儀器網(wǎng)
            供貨周期 一周 規(guī)格 T25
            貨號 EOMA 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥/生物制藥
            主要用途 科學(xué)研究
            CRL-2586 EOMA 小鼠血管內(nèi)皮瘤細(xì)胞,ATCC 細(xì)胞|細(xì)胞系|細(xì)胞株|腫瘤細(xì)胞|細(xì)胞|貼壁細(xì)胞|懸浮細(xì)胞|,細(xì)胞庫管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)優(yōu)培養(yǎng)條件,

            CRL-2586 EOMA 小鼠血管內(nèi)皮瘤細(xì)胞 的詳細(xì)介紹

            ATCC® Number:CRL-2586™  Price:$329.00
            Designations:EOMA

            Depositors:R Auerbach

            Biosafety Level:1

            Shipped:frozen

            Medium & Serum:See Propagation

            Growth Properties:adherent

            Organism:Mus musculus (mouse)

            Morphology:endothelial


            Source:Disease: hemangioendothelioma
            Strain: 129
            Cell Type: endothelial


            Cellular Products:angiotensin converting enzyme (ACE) [51514]

            thrombospondin [51514]

            cathepsin L [47148]

            endostatin [47148]

            interleukin-6 (interleukin 6, IL-6) [53484]



            Permits/Forms:In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
            CRL-2586 EOMA 小鼠血管內(nèi)皮瘤細(xì)胞

            Isolation:Isolation date: 1980

            Receptors:acetylated low density liproprotein [51514]

            Tumorigenic:Yes

            Antigen Expression:CD31 +

            vascular addressin +

            CD45 (Ly5-T200) +



            Age:adult

            Comments:The EOMA cell line was originally derived in 1980 from a mixed hemangioendothelioma arising in an adult mouse. [51514]

            The cells synthesize angiotensin-converting enzyme, express surface receptors for acetylated low density lipoprotein, produce thrombospondin and show intracellular staining with an antibody to von Willebrand factor. [51514]

            Cathepsin L is secreted by EOMA cells and is responsible for the generation of endostatin L. [47148]

            Although constitutive cytokine gene expression exists in EOMA cells, the level of IL-6 mRNA is prominently elevated by incubation with Liposome encapsulated hemoglobin (LEH). [53484]

            The cells constitutively express the vascular addressin identified by antibody MECA-99.

            EOMA cells exhibit characteristic endothelial cell properties, such as rearrangement into tubelike structures on Matrigel and retention of cobblestone morphology at confluence. They behave in vitro in a manner similar to microvascular endothelial cells. [51514]



            Propagation:ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's 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%.
            Temperature: 37.0°C


            Subculturing:Protocol:
            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.

            CRL-2586
            Subc*tion Ratio: A subc*tion ratio of 1:3 to 1:6 is recommended
            Medium Renewal: Every 2 to 3 days


            Preservation:Freeze medium: Complete growth medium supplemented with 5% DMSO
            Storage temperature: liquid nitrogen vapor phase


            Related Products:Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002

            recommended serum:ATCC 30-2020

            derivative:ATCC CRL-2587



            References:47148: Felbor U, et al. Secreted cathepsin L generates endostatin from collagen XVIII. EMBO J. 19: 1187-1194, 2000. PubMed: 10716919

            51514: Obeso J, et al. A hemangioendothelioma-derived cell line: its use as a model for the study of endothelial cell biology. Lab. Invest. 63: 259-269, 1990. PubMed: 2166185

            53484: Zhu XL, et al. Kinetics of cytokine gene expression in macrophage and endothelial cell lines following liposome encapsulated haemoglobin (LEH) treatment in vitro. Cytokine 8: 541-547, 1996. PubMed: 8891435

            53486: Wen W, et al. The generation of endostatin is mediated by elastase.. Cancer Res. 59: 6052-6056, 1999. PubMed: 10626789


            ATCC® Number: CRL-2586™ Price: $329.00

            Designations: EOMA

            Depositors: R Auerbach

            Biosafety Level: 1

            Shipped: frozen

            Medium & Serum: See Propagation

            Growth Properties: adherent

            Organism: Mus musculus (mouse)

            Morphology: endothelial



            CRL-2586

            Source: Disease: hemangioendothelioma

            Strain: 129

            Cell Type: endothelial

            Cellular Products: angiotensin converting enzyme (ACE) [51514]

            thrombospondin [51514]

            cathepsin L [47148]

            endostatin [47148]

            interleukin-6 (interleukin 6, IL-6) [53484]

            Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.


            Isolation: Isolation date: 1980

            Receptors: acetylated low density liproprotein [51514]

            Tumorigenic: Yes

            Antigen Expression: CD31 +

            vascular addressin +

            CD45 (Ly5-T200) +

            Age: adult

            Comments: The EOMA cell line was originally derived in 1980 from a mixed hemangioendothelioma arising in an adult mouse. [51514]

            The cells synthesize angiotensin-converting enzyme, express surface receptors for acetylated low density lipoprotein, produce thrombospondin and show intracellular staining with an antibody to von Willebrand factor. [51514]

            Cathepsin L is secreted by EOMA cells and is responsible for the generation of endostatin L. [47148]

            Although constitutive cytokine gene expression exists in EOMA cells, the level of IL-6 mRNA is prominently elevated by incubation with Liposome encapsulated hemoglobin (LEH). [53484]

            The cells constitutively express the vascular addressin identified by antibody MECA-99.

            EOMA cells exhibit characteristic endothelial cell properties, such as rearrangement into tubelike structures on Matrigel and retention of cobblestone morphology at confluence. They behave in vitro in a manner similar to microvascular endothelial cells. [51514]

            Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's 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%.

            Temperature: 37.0°C

            Subculturing: Protocol:

            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).


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