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    购宝钱包APP /科研细胞 /人源细胞系 /血液 /LAMA-84(人急变期慢性粒细胞白血病)

    LAMA-84(人急变期慢性粒细胞白血病)

    CBP61153

    询 价
    LAMA84细胞全景
    产品描述
    产品数据库
    I. General information 
    Synonyms: LAMA-84
    Background: established from the peripheral blood of a 29-year-old woman with chronic myeloid leukemia (CML) (treated 5 years with busulfan from 1979-1984) one month after onset of myeloid-megakaryocytic blast crisis; cells were described in the literature to express megakaryocytic and erythroid markers and to respond to induction of differentiation with various reagents; parental cell line of subclone LAMA-87 (DSM ACC 270); cells carry t(9;22) leading to BCR-ABL1 e14-a2 (b3-a2) fusion gene
    Species: human (Homo sapiens)
    Tissue: N/A 
    Disease: chronic myeloid leukemia in blast crisis
    Gender: N/A 
    Morphology: single, round to polymorph cells growing in suspension, some cells are loosely adherent with a spindle-like morphology;
    Growth Mode: N/A 
    Doubling Time: ca. 50 hours
    DNA Profile: N/A
    Our Cell Line Authentication Service
    Culture Medium:

    RPMI-1640+20%FBS

    LAMA-84完全培养基,# CBP61153M
    We strongly suggest to purchase the complete medium from us.

    Cryopreservation medium: 90%FBS+10%DMSO
    Mycoplasma: negative in DAPI, microbiological culture, RNA hybridization, PCR assays
    Immunology: CD3 -, CD11b +, CD13 +, CD15 -, CD19 -, CD33 +; 
    Fingerprint: unique DNA profile using multiplex PCR at D1S80, D2S44, D17S5 and ApoB
    Species: confirmed as human with IEF of AST, MDH
    Cytogenetics: human hypertriploid karyotype with 3.6% polyploidy - 73/74(69-77)<3n>XX, -X, +1, -2, +5, +6, +8, +13, -14, +17, +17, -18, +22, +mar, del(7)(p15), der(9)t(9;22)(q34;q11)x2, i(11q), add(13)(q33), del(17)(p12), der(22)t(9;22)(q34;q11)x4 - carries Ph (4 copies) - resembles published karyotype
    Molec. Genetics: expression of fusion gene BCR-ABL1 e14-a2 (b3-a2) confirmed by RT-PCR
    Virus   ELISA: reverse transcriptase negative; PCR: EBV -, HBV -, HCV -, HHV-8 -, HIV-1 -, HIV-2 -, HTLV-I/II -, MLV -, SMRV -
    Comments: For more information, please contact us (4008-750-250).

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