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human bone marrow mononuclear cell isolation kit  (Beijing Solarbio Science)


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    Beijing Solarbio Science human bone marrow mononuclear cell isolation kit
    Human Bone Marrow Mononuclear Cell Isolation Kit, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+bone+marrow+mononuclear+cell+isolation+kit/Human+Bone+Marrow+Mononuclear+Cell+Isolation+Solution+Kit/pmc12992729-103-9-17
    Average 94 stars, based on 5 article reviews
    human bone marrow mononuclear cell isolation kit - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Isolation:

    Article Title: NR2F2/AGAP2 axis: regulating lipid synthesis to drive AML progression via AMPKα/ACC pathway.
    Article Snippet: .. CD34 + cells were isolated from bone morrow using human bone marrow mononuclear cell isolation kit (#P8560, Solarbio, Beijing, China). ..

    Article Title: NR2F2/AGAP2 axis: regulating lipid synthesis to drive AML progression via AMPKα/ACC pathway
    Article Snippet: .. CD34 + cells were isolated from bone morrow using human bone marrow mononuclear cell isolation kit (#P8560, Solarbio, Beijing, China). ..

    Cell Isolation:

    Article Title: NR2F2/AGAP2 axis: regulating lipid synthesis to drive AML progression via AMPKα/ACC pathway.
    Article Snippet: .. CD34 + cells were isolated from bone morrow using human bone marrow mononuclear cell isolation kit (#P8560, Solarbio, Beijing, China). ..

    Article Title: NR2F2/AGAP2 axis: regulating lipid synthesis to drive AML progression via AMPKα/ACC pathway
    Article Snippet: .. CD34 + cells were isolated from bone morrow using human bone marrow mononuclear cell isolation kit (#P8560, Solarbio, Beijing, China). ..



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    human bone marrow mononuclear cells  (Beijing Solarbio Science)
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    Expression of RanBP3 is up-regulated in CML. (A) The RanBP3 mRNA level was analyzed in database GSE33075, including 9 healthy individuals and 9 CML patients. After removing the outliers of each group, 7 samples of each group were used for expression analysis. (B) Bone marrow <t>mononuclear</t> cells separated from 3 normal controls and 4 CML patients were used to assess the mRNA levels of RanBP3. (C) The protein levels of RanBP3 were detected in BCR-ABL positive cells K562, K562/G01, KCL22 and BCR-ABL negative cells HL60, THP-1 and NB4. (E) The protein levels of RanBP3 in BCR-ABL transformed mouse cell lines and their corresponding control cells. (D, F) The mRNA levels of RanBP3 correspond to cells in (C) and (E) . (G, H) K562 and K562/G01 cells were treated with various concentrations of IM for 48 hours and the protein (G) and mRNA (H) levels of RanBP3 in these cells were detected. **P < 0.01, ***P < 0.001.
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    Expression of RanBP3 is up-regulated in CML. (A) The RanBP3 mRNA level was analyzed in database GSE33075, including 9 healthy individuals and 9 CML patients. After removing the outliers of each group, 7 samples of each group were used for expression analysis. (B) Bone marrow mononuclear cells separated from 3 normal controls and 4 CML patients were used to assess the mRNA levels of RanBP3. (C) The protein levels of RanBP3 were detected in BCR-ABL positive cells K562, K562/G01, KCL22 and BCR-ABL negative cells HL60, THP-1 and NB4. (E) The protein levels of RanBP3 in BCR-ABL transformed mouse cell lines and their corresponding control cells. (D, F) The mRNA levels of RanBP3 correspond to cells in (C) and (E) . (G, H) K562 and K562/G01 cells were treated with various concentrations of IM for 48 hours and the protein (G) and mRNA (H) levels of RanBP3 in these cells were detected. **P < 0.01, ***P < 0.001.

    Journal: Frontiers in Oncology

    Article Title: RanBP3 Regulates Proliferation, Apoptosis and Chemosensitivity of Chronic Myeloid Leukemia Cells via Mediating SMAD2/3 and ERK1/2 Nuclear Transport

    doi: 10.3389/fonc.2021.698410

    Figure Lengend Snippet: Expression of RanBP3 is up-regulated in CML. (A) The RanBP3 mRNA level was analyzed in database GSE33075, including 9 healthy individuals and 9 CML patients. After removing the outliers of each group, 7 samples of each group were used for expression analysis. (B) Bone marrow mononuclear cells separated from 3 normal controls and 4 CML patients were used to assess the mRNA levels of RanBP3. (C) The protein levels of RanBP3 were detected in BCR-ABL positive cells K562, K562/G01, KCL22 and BCR-ABL negative cells HL60, THP-1 and NB4. (E) The protein levels of RanBP3 in BCR-ABL transformed mouse cell lines and their corresponding control cells. (D, F) The mRNA levels of RanBP3 correspond to cells in (C) and (E) . (G, H) K562 and K562/G01 cells were treated with various concentrations of IM for 48 hours and the protein (G) and mRNA (H) levels of RanBP3 in these cells were detected. **P < 0.01, ***P < 0.001.

    Article Snippet: Mononuclear cells were separated following the instructions of the human bone marrow mononuclear cells (BMMCs) separation regents (Solarbio, China).

    Techniques: Expressing, Transformation Assay, Control