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mouse anti- idh1-r132h  (Biozol Diagnostica Vertrieb GmbH)
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Humanin is strongly expressed in hGBMs (A) Myeloid cells purified from biopsies of epilepsy surgery (tumor free) or GBMs underwent transcriptomic profiling and bioinformatics analysis. (B) The mitochondrial ribosomal RNA-encoding gene MT-RNR2 is among the top-5 upregulated genes in GAMs. MT-RNR2 contains an open reading frame for the peptide humanin. (C) Confocal microscopy of GBMs immunolabeled for humanin and the myeloid cell marker Iba1; GAMs expressing humanin are indicated (arrowheads). (D) A single optical section of GAMs (arrow) and other intratumoral cells (double arrow) plus confocal cross hair inspection (insert). (E) Immunofluorescence labeling for humanin in GBMs and controls was quantified (dots indicating individual patient samples). (F) In <t>IDH1-mutant</t> (IDH1 <t>R132H</t> ), grade-IV astrocytomas, humanin expression is largely confined to GBM cells. The number of biological replicates is indicated (each dot in the graph indicates average data from one individual sample); error bars are presented as mean ± SDM. Statistical significance is shown as false discovery rate (FDR) in (A) and by t test (∗∗∗∗ p < 0.0001) in (E); scales indicate 30 μm (C), 10 μm (D, F).
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Humanin is strongly expressed in hGBMs (A) Myeloid cells purified from biopsies of epilepsy surgery (tumor free) or GBMs underwent transcriptomic profiling and bioinformatics analysis. (B) The mitochondrial ribosomal RNA-encoding gene MT-RNR2 is among the top-5 upregulated genes in GAMs. MT-RNR2 contains an open reading frame for the peptide humanin. (C) Confocal microscopy of GBMs immunolabeled for humanin and the myeloid cell marker Iba1; GAMs expressing humanin are indicated (arrowheads). (D) A single optical section of GAMs (arrow) and other intratumoral cells (double arrow) plus confocal cross hair inspection (insert). (E) Immunofluorescence labeling for humanin in GBMs and controls was quantified (dots indicating individual patient samples). (F) In <t>IDH1-mutant</t> (IDH1 <t>R132H</t> ), grade-IV astrocytomas, humanin expression is largely confined to GBM cells. The number of biological replicates is indicated (each dot in the graph indicates average data from one individual sample); error bars are presented as mean ± SDM. Statistical significance is shown as false discovery rate (FDR) in (A) and by t test (∗∗∗∗ p < 0.0001) in (E); scales indicate 30 μm (C), 10 μm (D, F).
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mouse anti idh1 antibody  (Santa Cruz Biotechnology)
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Humanin is strongly expressed in hGBMs (A) Myeloid cells purified from biopsies of epilepsy surgery (tumor free) or GBMs underwent transcriptomic profiling and bioinformatics analysis. (B) The mitochondrial ribosomal RNA-encoding gene MT-RNR2 is among the top-5 upregulated genes in GAMs. MT-RNR2 contains an open reading frame for the peptide humanin. (C) Confocal microscopy of GBMs immunolabeled for humanin and the myeloid cell marker Iba1; GAMs expressing humanin are indicated (arrowheads). (D) A single optical section of GAMs (arrow) and other intratumoral cells (double arrow) plus confocal cross hair inspection (insert). (E) Immunofluorescence labeling for humanin in GBMs and controls was quantified (dots indicating individual patient samples). (F) In <t>IDH1-mutant</t> (IDH1 <t>R132H</t> ), grade-IV astrocytomas, humanin expression is largely confined to GBM cells. The number of biological replicates is indicated (each dot in the graph indicates average data from one individual sample); error bars are presented as mean ± SDM. Statistical significance is shown as false discovery rate (FDR) in (A) and by t test (∗∗∗∗ p < 0.0001) in (E); scales indicate 30 μm (C), 10 μm (D, F).
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Humanin is strongly expressed in hGBMs (A) Myeloid cells purified from biopsies of epilepsy surgery (tumor free) or GBMs underwent transcriptomic profiling and bioinformatics analysis. (B) The mitochondrial ribosomal RNA-encoding gene MT-RNR2 is among the top-5 upregulated genes in GAMs. MT-RNR2 contains an open reading frame for the peptide humanin. (C) Confocal microscopy of GBMs immunolabeled for humanin and the myeloid cell marker Iba1; GAMs expressing humanin are indicated (arrowheads). (D) A single optical section of GAMs (arrow) and other intratumoral cells (double arrow) plus confocal cross hair inspection (insert). (E) Immunofluorescence labeling for humanin in GBMs and controls was quantified (dots indicating individual patient samples). (F) In <t>IDH1-mutant</t> (IDH1 <t>R132H</t> ), grade-IV astrocytomas, humanin expression is largely confined to GBM cells. The number of biological replicates is indicated (each dot in the graph indicates average data from one individual sample); error bars are presented as mean ± SDM. Statistical significance is shown as false discovery rate (FDR) in (A) and by t test (∗∗∗∗ p < 0.0001) in (E); scales indicate 30 μm (C), 10 μm (D, F).
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mouse anti-idh1 r132h - by Bioz Stars, 2026-09
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Humanin is strongly expressed in hGBMs (A) Myeloid cells purified from biopsies of epilepsy surgery (tumor free) or GBMs underwent transcriptomic profiling and bioinformatics analysis. (B) The mitochondrial ribosomal RNA-encoding gene MT-RNR2 is among the top-5 upregulated genes in GAMs. MT-RNR2 contains an open reading frame for the peptide humanin. (C) Confocal microscopy of GBMs immunolabeled for humanin and the myeloid cell marker Iba1; GAMs expressing humanin are indicated (arrowheads). (D) A single optical section of GAMs (arrow) and other intratumoral cells (double arrow) plus confocal cross hair inspection (insert). (E) Immunofluorescence labeling for humanin in GBMs and controls was quantified (dots indicating individual patient samples). (F) In IDH1-mutant (IDH1 R132H ), grade-IV astrocytomas, humanin expression is largely confined to GBM cells. The number of biological replicates is indicated (each dot in the graph indicates average data from one individual sample); error bars are presented as mean ± SDM. Statistical significance is shown as false discovery rate (FDR) in (A) and by t test (∗∗∗∗ p < 0.0001) in (E); scales indicate 30 μm (C), 10 μm (D, F).

Journal: Cell Reports Medicine

Article Title: Myeloid cells coordinately induce glioma cell-intrinsic and cell-extrinsic pathways for chemoresistance via GP130 signaling

doi: 10.1016/j.xcrm.2024.101658

Figure Lengend Snippet: Humanin is strongly expressed in hGBMs (A) Myeloid cells purified from biopsies of epilepsy surgery (tumor free) or GBMs underwent transcriptomic profiling and bioinformatics analysis. (B) The mitochondrial ribosomal RNA-encoding gene MT-RNR2 is among the top-5 upregulated genes in GAMs. MT-RNR2 contains an open reading frame for the peptide humanin. (C) Confocal microscopy of GBMs immunolabeled for humanin and the myeloid cell marker Iba1; GAMs expressing humanin are indicated (arrowheads). (D) A single optical section of GAMs (arrow) and other intratumoral cells (double arrow) plus confocal cross hair inspection (insert). (E) Immunofluorescence labeling for humanin in GBMs and controls was quantified (dots indicating individual patient samples). (F) In IDH1-mutant (IDH1 R132H ), grade-IV astrocytomas, humanin expression is largely confined to GBM cells. The number of biological replicates is indicated (each dot in the graph indicates average data from one individual sample); error bars are presented as mean ± SDM. Statistical significance is shown as false discovery rate (FDR) in (A) and by t test (∗∗∗∗ p < 0.0001) in (E); scales indicate 30 μm (C), 10 μm (D, F).

Article Snippet: Mouse anti- IDH1-R132H , Dianova , Cat# DIA-H09, RRID: AB_2335716.

Techniques: Purification, Confocal Microscopy, Immunolabeling, Marker, Expressing, Immunofluorescence, Labeling, Mutagenesis

Journal: Cell Reports Medicine

Article Title: Myeloid cells coordinately induce glioma cell-intrinsic and cell-extrinsic pathways for chemoresistance via GP130 signaling

doi: 10.1016/j.xcrm.2024.101658

Figure Lengend Snippet:

Article Snippet: Mouse anti- IDH1-R132H , Dianova , Cat# DIA-H09, RRID: AB_2335716.

Techniques: Plasmid Preparation, Recombinant, Transfection, Fluorescence, Staining, Reverse Transcription, Expressing, Liposomes, Mutagenesis, shRNA, Control, Construct, Software, Imaging, Functional Assay, Dissection, Sequencing, Real-time Polymerase Chain Reaction