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            HTB-125 Hs 578Bst 人正常乳腺細胞

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            更新時間:2024-11-16 16:11:43瀏覽次數(shù):1987

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            供貨周期 一周 貨號 Hs 578Bst
            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
            HTB-125 Hs 578Bst 人正常乳腺細胞, ATCC 細胞|細胞系|細胞株|腫瘤細胞|細胞;細胞庫管理規(guī)范,提供的細胞株背景清楚,提供參考文獻和培養(yǎng)條件!

            HTB-125 Hs 578Bst 人正常乳腺細胞

            OrganismHomo sapiens, human
            Tissuemammary gland/breast
            Cell TypeEpithelial, Myoepithelial
            Product Formatfrozen
            Morphologyfibroblast
            Culture Propertiesadherent
            Biosafety Level1
            Diseasenormal
            Age74 years
            Genderfemale
            EthnicityCaucasian            

            HTB-125 Hs 578Bst 人正常乳腺細胞

            Storage Conditionsliquid nitrogen vapor phase
            Karyotypemodal number . Both X = 46; range = 42 to 48

            This is a diploid human cell line with 46,XX karyotype. Polyploidy occurred at 6.9%chromosomes were normal. The chromosome N9 pair was heteromorphic for the centromeric heterochromatin having one with the normal size and the other about twice the size of the normal.



            Derivation

            Hs 578Bst was derived by A.J. Hackett, et al. from normal breast tissue peripheral to an infiltrating ductal carcinoma which was the source for Hs 578T (see ATCC HTB-126).

            Hs 578Bst may have been myoepithelial in origin since the cells possessed microfilaments and clusters of pinocytotic vesicles similar to those seen in myoepithelia in vivo.


            Receptor ExpressionEpidermal growth factor (EGF)


            Comments

            No desmosomes were observed, estrogen receptor protein was not present, and no endogenous viruses were detected.

            A frozen ampule at unknown population doubling (PDL) was received at the ATCC in 1983. Cells had the potential to reach approximay 22 more population doublings before the onset of senescence. See Batch Specific information for PDL of current Distribution freeze.

            Complete Growth MediumThe base medium for this cell line is ATCC Hybri-Care Medium, Catalog No. 46-X. Hybri-Care Medium is supplied as a powder and should be reconstituted in 1 L cell-culture-grade water and supplemented with 1.5 g/L sodium bicarbonate. To make the complete growth medium, add the following components to the base medium: 30 ng/ml mouse EGF; fetal bovine serum to a final concentration of 10%.
            Subculturing

            Volumes used in this protocol are for 75 cm2 flasks; 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-0.53mM EDTA solution to remove all traces of serum which 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.


            Medium Renewal: 2 to 3 times per week



            Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 13 in Culture Of Animal Cells: A Manual Of Basic Technique by R. Ian Freshney, 5th edition, published by Wiley-Liss, N.Y., 2005.

            CryopreservationComplete growth medium, 95%; DMSO, 5%. Cell culture tested DMSO is available as ATCC Catalog No. 4-X.


            Culture Conditions

            Temperature: 37°C

            Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
















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