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                SK-N-SH(神经母细胞瘤细胞)

                SK-N-SH(神经母细胞瘤细胞)
                <
                • SK-N-SH(神经母细胞瘤细胞)
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                ATCC
                HTB-11 (株)
                上海锐聪科技发展有限公司
                上海
                详细说明

                SK-N-SH(神经母细胞瘤细胞)

                SK-N-SH(神经母细胞瘤细胞)
                 
                Cell Biology
                ATCC® Number: HTB-11™ Price: $203.00
                Designations:
                SK-N-SH
                Depositors:
                G Trempe
                LJ Old
                1
                Shipped:
                frozen
                Medium & Serum:
                Growth Properties:
                adherent
                Organism:
                Homo sapiens (human)
                Morphology:
                epithelial
                SK-N-SH(神经母细胞瘤细胞)
                 
                Source:
                Organ: brain
                Disease: neuroblastoma
                Derived from metastatic site: bone marrow
                Cellular Products:
                plasminogen activator,shows increased expression of M-CSF after treatment with amyloid-beta peptide
                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 ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
                Restrictions:
                The cells are distributed for research purposes only. The Memorial Sloan-Kettering Cancer Center releases the line subject to the following: 1.) The cells or their products must not be distributed to third parties. Commercial interests are the exclusive property of Memorial Sloan-Kettering Cancer Center. 2.) Any proposed commercial use of these cells must first be negotiated with The Director, Office of Industrial Affairs, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; phone (212) 639-6181; FAX (212) 717-3439.
                Applications:
                transfection host (technology from amaxa)
                Antigen Expression:
                Blood Type A; Rh+
                DNA Profile
                (STR):
                Amelogenin: X
                CSF1PO: 11
                D13S317: 11
                D16S539: 8,13
                D5S818: 12
                D7S820: 7,10
                THO1: 7,10
                TPOX: 8,11
                vWA: 14,18
                Cytogenetic
                Analysis:
                The cell line is hyperdiploid human female (XX), with the modal chromosome number of 47. Normal chromosomes N9 and N22 are single. One copy of each of these chromosomes is structurally altered to form the two marker chromosomes 9q+ and 22q+.
                Chromosomes N7 is trisomic. Extra bands were found on one copy of chromosome N7, thereby forming a marker chromosome as described by R.C. Seeger. May have been translocated in part(s) to the q arms of chromosomes N9 and N22. [26318]
                Isoenzymes:
                AK-1, 1; ES-D, 1; G6PD, B; GLO-I, 1; Me-2, 2; PGM1, 1; PGM3, 1
                Age:
                4 years
                Gender:
                female
                Comments:
                The SK-N-SH line was developed by J.L. Biedler and differs from SK-N-MC (see ATCC HTB-10) in that it exhibits a longer doubling time and higher levels of dopamine - beta - hydroxylase.
                SK-N-SH has been used as a target cell line in cell mediated cytotoxicity assays.
                Propagation:
                ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagles Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
                Temperature: 37.0C
                Subculturing:
                Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach.
                Add fresh culture medium, aspirate and dispense into new culture flasks.
                Subcultivation ratio: A subcultivation ratio of 1:3 to 1:8 is recommended

                Medium renewal: 1 to 2 times per week
                Preservation:
                Culture medium, 95%; DMSO, 5%
                Related Products:
                Recommended medium (without the additional supplements or serum described under ATCC Medium): ATCC 30-2003
                recommended serum: ATCC 30-2020
                References:
                1191: Gilbert LC , Wachsman JT . Characterization and partial purification of the plasminogen activator from human neuroblastoma cell line, SK-N-SH. A comparison with human urokinase. Biochim. Biophys. Acta 704: 450-460, 1982. PubMed:
                2154: Spengler BA , et al.. Morphology and growth, tumorigenicity, and cytogenetics of human neuroblastoma cells established in vitro. In Vitro 8: 410, 1973.
                22536: Fogh J , et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871
                23260: Bluestein HG . Neurocytotoxic antibodies in serum of patients with systemic lupus erythematosus. Proc. Natl. Acad. Sci. USA 75: 3965-3969, 1978. PubMed: 279013
                26318: Seeger RC , et al. Morphology, growth, chromosomal pattern and fibrinolytic activity of two new human neuroblastoma cell lines. Cancer Res. 37: 1364-1371, 1977. PubMed: 856461
                29165: Yan SD , et al. Amyloid-beta peptide-Receptor for Advanced Glycation Endproduct interaction elicits neuronal expression of macrophage-colony stimulating factor: A proinflammatory pathway in Alzheimer disease. Proc. Natl. Acad. Sci. USA 94: 5296-5301, 1997. PubMed:
                32265: Tsao H , et al. Novel mutations in the p16/CDKN2A binding region of the Cyclin-dependent Kinase-4 gene. Cancer Res. 58: 109-113, 1998. PubMed:
                32287: Rostomily RC , et al. Expression of neurogenic basic helix-loop-helix genes in primitive neuroectodermal tumors. Cancer Res. 57: 3526-3531, 1997. PubMed:
                32524: Chang YE , et al. Properties of the protein encoded by the UL32 open reading frame of herpes simplex virus 1. J. Virol. 70: 3938-3946, 1996. PubMed:
                32725: He B , et al. The carboxyl terminus of the murine MyD116 gene substitutes for the corresponding domain of the gamma134.5 gene of herpes simplex virus to preclude the premature shutoff of total protein synthesis in infected human cells. J. Virol. 70: 84-90, 1996. PubMed:
                32757: Yoshikawa T , et al. Downstream regulatory elements increase acute and latent herpes simplex virus type 2 latency-associated transcript expression but do not influence recurrence phenotype or establishment of latency. J. Virol. 70: 1535-1541, 1996. PubMed:

                 

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