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human bmp5 recombinant protein  (MedChemExpress)


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    MedChemExpress human bmp5 recombinant protein
    Human Bmp5 Recombinant Protein, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+bmp5+protein/BMP-5%2C+Human/pm41760598-238-14-21
    Average 94 stars, based on 3 article reviews
    human bmp5 recombinant protein - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Recombinant:

    Article Title: Identification of GLDN + odontogenic stem cells as crucial for human tooth development and regeneration.
    Article Snippet: After 4 h of incubation at 37 °C, images were collected and analyzed using ImageJ software to assess the tube formation ability of HUVECs in each group. .. Recombinant BMP5 protein In the cell proliferation, migration, tube formation, and osteogenic induction assays, human BMP5 recombinant protein (HEK293, hFc) (#HY-P75472; MCE) was added to the culture medium or osteogenic induction medium at the onset of the experiment and maintained throughout. ..

    Migration:

    Article Title: Identification of GLDN + odontogenic stem cells as crucial for human tooth development and regeneration.
    Article Snippet: After 4 h of incubation at 37 °C, images were collected and analyzed using ImageJ software to assess the tube formation ability of HUVECs in each group. .. Recombinant BMP5 protein In the cell proliferation, migration, tube formation, and osteogenic induction assays, human BMP5 recombinant protein (HEK293, hFc) (#HY-P75472; MCE) was added to the culture medium or osteogenic induction medium at the onset of the experiment and maintained throughout. ..



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    G9a knockdown may lead to increase in <t>BMP5</t> expression. ( A ) Regulatory factors suppressing tumor aggressiveness were identified by using microarray analysis. ( B ) Expression levels for each gene were compared (ratios between gene expression levels of non-silencing control). In two G9a knockdown cells (shG9a #1 and shG9a #2), expression levels for each gene were compared to those of non-silencing control. Then the most upregulated and downregulated genes were screened. ( C ) G9a knockdown cells showed increase in BMP5 expression. ( D ) Reduced G9a occupancy was found at the BMP5 promoter region. G9a knockdown cells also showed decreased H3K9me2 occupancy at the promoter region of BMP5. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.
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    Illustration of selective components in the <t>BMP</t> <t>signaling</t> pathway, important for bone and cartilage formation and fracture healing. Bone morphogenetic proteins (BMP) induce intracellular signaling by binding the transmembrane receptors BMPR-II and BMPR-I. When these serine/threonine receptors are activated by BMPs, BMPR-I becomes phosphorylated. When both BMPR-II and BMPR-I are bound to BMPs and phosphorylated, downstream signaling is activated via the phosphorylation of transcription factors SMAD 1/5/8. Activated pSMAD 1/5/8 forms a complex with cofactor SMAD4, allowing for the regulated transcription of downstream target genes.
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    G9a knockdown may lead to increase in BMP5 expression. ( A ) Regulatory factors suppressing tumor aggressiveness were identified by using microarray analysis. ( B ) Expression levels for each gene were compared (ratios between gene expression levels of non-silencing control). In two G9a knockdown cells (shG9a #1 and shG9a #2), expression levels for each gene were compared to those of non-silencing control. Then the most upregulated and downregulated genes were screened. ( C ) G9a knockdown cells showed increase in BMP5 expression. ( D ) Reduced G9a occupancy was found at the BMP5 promoter region. G9a knockdown cells also showed decreased H3K9me2 occupancy at the promoter region of BMP5. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Journal: International Journal of Molecular Sciences

    Article Title: G9a Knockdown Suppresses Cancer Aggressiveness by Facilitating Smad Protein Phosphorylation through Increasing BMP5 Expression in Luminal A Type Breast Cancer

    doi: 10.3390/ijms23020589

    Figure Lengend Snippet: G9a knockdown may lead to increase in BMP5 expression. ( A ) Regulatory factors suppressing tumor aggressiveness were identified by using microarray analysis. ( B ) Expression levels for each gene were compared (ratios between gene expression levels of non-silencing control). In two G9a knockdown cells (shG9a #1 and shG9a #2), expression levels for each gene were compared to those of non-silencing control. Then the most upregulated and downregulated genes were screened. ( C ) G9a knockdown cells showed increase in BMP5 expression. ( D ) Reduced G9a occupancy was found at the BMP5 promoter region. G9a knockdown cells also showed decreased H3K9me2 occupancy at the promoter region of BMP5. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Article Snippet: Recombinant human BMP5 (#615-BMC-020, R&D Systems, Minneapolis, MN, USA) was reconstituted at 100 ug/mL in 4 mM HCl containing 0.1% BSA.

    Techniques: Knockdown, Expressing, Microarray, Gene Expression, Control

    BMP5 contributes to reduce migration and invasion abilities of tumor cells. ( A ) Low BMP5 expression is associated with poor survival outcomes of breast cancer patients. ( B ) Patients with stage 3 disease showed higher BMP5 levels than those of stage 2 patients. ( C , D ) Migration/invasion abilities were decreased by treatment of recombinant BMP5; however, the capabilities were enhanced following BMP5 downregulation. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, **** p < 0.0001.

    Journal: International Journal of Molecular Sciences

    Article Title: G9a Knockdown Suppresses Cancer Aggressiveness by Facilitating Smad Protein Phosphorylation through Increasing BMP5 Expression in Luminal A Type Breast Cancer

    doi: 10.3390/ijms23020589

    Figure Lengend Snippet: BMP5 contributes to reduce migration and invasion abilities of tumor cells. ( A ) Low BMP5 expression is associated with poor survival outcomes of breast cancer patients. ( B ) Patients with stage 3 disease showed higher BMP5 levels than those of stage 2 patients. ( C , D ) Migration/invasion abilities were decreased by treatment of recombinant BMP5; however, the capabilities were enhanced following BMP5 downregulation. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, **** p < 0.0001.

    Article Snippet: Recombinant human BMP5 (#615-BMC-020, R&D Systems, Minneapolis, MN, USA) was reconstituted at 100 ug/mL in 4 mM HCl containing 0.1% BSA.

    Techniques: Migration, Expressing, Recombinant

    G9a knockdown facilitates Smad protein phosphorylation via BMP5 activation. ( A , B ) G9a-knockdown-induced increase in BMP5 expression had no effect on the total level of either Smad1 or Smad5. G9a knockdown increased phosphorylation of Smad1/5/9. ( C ) ICC demonstrated that nuclear translocation of pSmad1/5/9 was increased in G9a-depleted MCF7 cells. ( D ) Similar tendency was found after treatment of recombinant BMP5. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, ns = not significant.

    Journal: International Journal of Molecular Sciences

    Article Title: G9a Knockdown Suppresses Cancer Aggressiveness by Facilitating Smad Protein Phosphorylation through Increasing BMP5 Expression in Luminal A Type Breast Cancer

    doi: 10.3390/ijms23020589

    Figure Lengend Snippet: G9a knockdown facilitates Smad protein phosphorylation via BMP5 activation. ( A , B ) G9a-knockdown-induced increase in BMP5 expression had no effect on the total level of either Smad1 or Smad5. G9a knockdown increased phosphorylation of Smad1/5/9. ( C ) ICC demonstrated that nuclear translocation of pSmad1/5/9 was increased in G9a-depleted MCF7 cells. ( D ) Similar tendency was found after treatment of recombinant BMP5. p values were calculated using ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, ns = not significant.

    Article Snippet: Recombinant human BMP5 (#615-BMC-020, R&D Systems, Minneapolis, MN, USA) was reconstituted at 100 ug/mL in 4 mM HCl containing 0.1% BSA.

    Techniques: Knockdown, Phospho-proteomics, Activation Assay, Expressing, Translocation Assay, Recombinant

    Illustration of selective components in the BMP signaling pathway, important for bone and cartilage formation and fracture healing. Bone morphogenetic proteins (BMP) induce intracellular signaling by binding the transmembrane receptors BMPR-II and BMPR-I. When these serine/threonine receptors are activated by BMPs, BMPR-I becomes phosphorylated. When both BMPR-II and BMPR-I are bound to BMPs and phosphorylated, downstream signaling is activated via the phosphorylation of transcription factors SMAD 1/5/8. Activated pSMAD 1/5/8 forms a complex with cofactor SMAD4, allowing for the regulated transcription of downstream target genes.

    Journal: Journal of orthopaedic trauma

    Article Title: The Effects of Episodic Alcohol Exposure on BMP2 Signaling During Tibia Fracture Healing

    doi: 10.1097/BOT.0000000000001160

    Figure Lengend Snippet: Illustration of selective components in the BMP signaling pathway, important for bone and cartilage formation and fracture healing. Bone morphogenetic proteins (BMP) induce intracellular signaling by binding the transmembrane receptors BMPR-II and BMPR-I. When these serine/threonine receptors are activated by BMPs, BMPR-I becomes phosphorylated. When both BMPR-II and BMPR-I are bound to BMPs and phosphorylated, downstream signaling is activated via the phosphorylation of transcription factors SMAD 1/5/8. Activated pSMAD 1/5/8 forms a complex with cofactor SMAD4, allowing for the regulated transcription of downstream target genes.

    Article Snippet: BMP Signaling Assays Protein expressions of BMP2, BMPRII, BMPR1A, and the inhibitor Chordin were all assessed via the following commercially available ELISA kits: BMP2 (Boster Biological Technology, EKO312, Pleasanton, CA); BMPRII (Mybiosource, MBS701412, San Diego, CA); BMPRIA (Mybiosource, MBS720872); Chordin (Mybiosource, MBS2021328).

    Techniques: Binding Assay, Phospho-proteomics