olig2 rabbit antibody Search Results


94
Bio-Techne corporation olig2 antibody - azide and bsa free
Olig2 Antibody Azide And Bsa Free, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/bio-techne+corporation___nbp1-28667?v=Bio-Techne+corporation
Average 94 stars, based on 1 article reviews
olig2 antibody - azide and bsa free - by Bioz Stars, 2026-07
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92
OriGene immunohistochemical ihc staining
Glial cells in EAE mice were consistently suppressed by VCAM-1− and VCAM-1 + hUC-MSCs a – b Representative <t>IHC</t> staining ( a ) and statistical analysis ( b ) showed the distribution of Gfap + astrocytes and Iba + microglia in spinal cord of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. c – d Representative IF staining ( c ) and statistical analysis ( d ) showed the distribution of Gfap + astrocytes and Iba + microglia in brain of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. Data were shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01, ***P < 0.001; ns, not significant
Immunohistochemical Ihc Staining, supplied by OriGene, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/pmc11607028-44-10-13?v=OriGene
Average 92 stars, based on 1 article reviews
immunohistochemical ihc staining - by Bioz Stars, 2026-07
92/100 stars
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90
IBL America anti-olig2
Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human <t>OLIG2+/SOX10+</t> CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).
Anti Olig2, supplied by IBL America, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/pmc06031359-311-32-36?v=IBL+America
Average 90 stars, based on 1 article reviews
anti-olig2 - by Bioz Stars, 2026-07
90/100 stars
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Abnova rabbit olig2 antibody
Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human <t>OLIG2+/SOX10+</t> CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).
Rabbit Olig2 Antibody, supplied by Abnova, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/pm23160237-518-82-85?v=Abnova
Average 90 stars, based on 1 article reviews
rabbit olig2 antibody - by Bioz Stars, 2026-07
90/100 stars
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90
Synaptic Systems guinea pig anti-olig2
Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human <t>OLIG2+/SOX10+</t> CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).
Guinea Pig Anti Olig2, supplied by Synaptic Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/pm40541184-517-29-33?v=Synaptic+Systems
Average 90 stars, based on 1 article reviews
guinea pig anti-olig2 - by Bioz Stars, 2026-07
90/100 stars
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90
Boster Bio olig2
Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human <t>OLIG2+/SOX10+</t> CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).
Olig2, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/pm33141073-86-19-20?v=Boster+Bio
Average 90 stars, based on 1 article reviews
olig2 - by Bioz Stars, 2026-07
90/100 stars
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94
Bio-Techne corporation human igsf3 antibody
Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human <t>OLIG2+/SOX10+</t> CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).
Human Igsf3 Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olig2+rabbit+antibody/bio-techne+corporation___af4788?v=Bio-Techne+corporation
Average 94 stars, based on 1 article reviews
human igsf3 antibody - by Bioz Stars, 2026-07
94/100 stars
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Rabbit Polyclonal OLIG2 Antibody
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N/A
Rabbit anti-Human OLIG2 Polyclonal Antibody
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N/A
Rabbit anti-Zebrafish olig2 Polyclonal Antibody
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N/A
Produced in rabbits immunized with purified a synthetic peptide corresponding to the N terminus of the Human Olig 2 Oligo2 and purified by antigen affinity chromatography
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N/A
Produced in rabbits immunized with a synthetic peptide corresponding to the C terminus of the Human Olig 2 and purified by antigen affinity chromatography
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Image Search Results


Glial cells in EAE mice were consistently suppressed by VCAM-1− and VCAM-1 + hUC-MSCs a – b Representative IHC staining ( a ) and statistical analysis ( b ) showed the distribution of Gfap + astrocytes and Iba + microglia in spinal cord of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. c – d Representative IF staining ( c ) and statistical analysis ( d ) showed the distribution of Gfap + astrocytes and Iba + microglia in brain of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. Data were shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01, ***P < 0.001; ns, not significant

Journal: Neurochemical Research

Article Title: VCAM-1 + Mesenchymal Stem/Stromal Cells Reveal Preferable Efficacy Upon an Experimental Autoimmune Encephalomyelitis Mouse Model of Multiple Sclerosis Over the VCAM-1 − Counterpart

doi: 10.1007/s11064-024-04267-w

Figure Lengend Snippet: Glial cells in EAE mice were consistently suppressed by VCAM-1− and VCAM-1 + hUC-MSCs a – b Representative IHC staining ( a ) and statistical analysis ( b ) showed the distribution of Gfap + astrocytes and Iba + microglia in spinal cord of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. c – d Representative IF staining ( c ) and statistical analysis ( d ) showed the distribution of Gfap + astrocytes and Iba + microglia in brain of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. Data were shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01, ***P < 0.001; ns, not significant

Article Snippet: The expression of neural and inflammatory biomarkers was detected by immunohistochemical (IHC) staining (Zsbio, Beijing, China) with the indicated antibodies (Iba, Gfap, CD45, CD68, Olig2).

Techniques: Immunohistochemistry, Staining

Inflammatory infiltrates in CNS of EAE mice was effectively alleviated by VCAM-1 − and VCAM-1 + hUC-MSCs infusion a Representative H&E staining showed the inflammatory infiltrates in the spinal cord of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. b Immunohistochemical (IHC) staining showed the content of CD45 + leukocytes and CD68 + macrophages in the spinal cord of mice in the aforementioned groups. Scale bar = 20 μm. c IHC staining showed the content of CD45 + leukocytes and CD68 + macrophages in the brain of mice in the aforementioned groups. Scale bar = 20 μm. d – e Statistical analysis of CD45 + area and CD68 + area in the spinal cord (d) and brain ( e ) of mice in the aforementioned groups. f – g qRT-PCR analysis showed the mRNA expression of proinflammatory factors (Ifn-γ, Tnf-α, Il-6, Il-1β) in spinal cord ( f ) and brain ( g ) of mice in the aforementioned groups. Data were shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001; ns, not significant

Journal: Neurochemical Research

Article Title: VCAM-1 + Mesenchymal Stem/Stromal Cells Reveal Preferable Efficacy Upon an Experimental Autoimmune Encephalomyelitis Mouse Model of Multiple Sclerosis Over the VCAM-1 − Counterpart

doi: 10.1007/s11064-024-04267-w

Figure Lengend Snippet: Inflammatory infiltrates in CNS of EAE mice was effectively alleviated by VCAM-1 − and VCAM-1 + hUC-MSCs infusion a Representative H&E staining showed the inflammatory infiltrates in the spinal cord of mice in the indicated groups (C, E, U, V). Scale bar = 20 μm. b Immunohistochemical (IHC) staining showed the content of CD45 + leukocytes and CD68 + macrophages in the spinal cord of mice in the aforementioned groups. Scale bar = 20 μm. c IHC staining showed the content of CD45 + leukocytes and CD68 + macrophages in the brain of mice in the aforementioned groups. Scale bar = 20 μm. d – e Statistical analysis of CD45 + area and CD68 + area in the spinal cord (d) and brain ( e ) of mice in the aforementioned groups. f – g qRT-PCR analysis showed the mRNA expression of proinflammatory factors (Ifn-γ, Tnf-α, Il-6, Il-1β) in spinal cord ( f ) and brain ( g ) of mice in the aforementioned groups. Data were shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001; ns, not significant

Article Snippet: The expression of neural and inflammatory biomarkers was detected by immunohistochemical (IHC) staining (Zsbio, Beijing, China) with the indicated antibodies (Iba, Gfap, CD45, CD68, Olig2).

Techniques: Staining, Immunohistochemical staining, Immunohistochemistry, Quantitative RT-PCR, Expressing

Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human OLIG2+/SOX10+ CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).

Journal: Disease Models & Mechanisms

Article Title: Epigenetic regulators Rbbp4 and Hdac1 are overexpressed in a zebrafish model of RB1 embryonal brain tumor, and are required for neural progenitor survival and proliferation

doi: 10.1242/dmm.034124

Figure Lengend Snippet: Zebrafish rb1 brain tumors express an oligoneural precursor signature similar to human OLIG2+/SOX10+ CNS-PNET. (A) Zebrafish rb1 brain tumor model created by somatic targeting of rb1 exon 2 with CRISPR-Cas9 or TALENs. Gross brain tumors develop in the midbrain and hindbrain (red asterisks) of adults at 4-5 months of age. For transcriptome analysis, half of the tumor tissue was dissected from ten tumor-positive fish for RNA isolation. The remaining tissue was embedded for pathology and immunolabeling. (B) Heat maps of log2(FPKM) show differential gene expression in zebrafish rb1 brain tumor transcriptome of 120 genes in the human OLIG2+/SOX10+ CNS-PNET subtype. rb1 tumor RNA-Seq of ten biological replicates from ten individual tumor positive adults, and C RNA-Seq of two biological replicates of three pooled normal adult zebrafish brain, are shown. (C-L) Histological and immunolabeling of wild-type adult zebrafish pretectum/diencephalon (C-G) and tumor-containing brain tissue from transcriptome individual T2 (H,I) and T8 (J-L). Neoplastic cells in T2 tumor show small densely basophilic nuclei, consistent with primitive neuroectodermal-like tumors (H,I). In normal adult brain, Olig2, Sox2 and Sox10 labeling is restricted to cells at or adjacent to the ventricle (E-G). High levels of Olig2, Sox2 and Sox10 are detected in the neoplastic tissue in tumor T8. Phosphohistone H3-labeled mitotic cells are scattered throughout the lesion (J-L). Scale bars: 200 µm (C,H); 50 µm (E,F,G,J,K,L).

Article Snippet: Cryosections were labeled with the following antibodies: rabbit polyclonal anti-phosphohistone H3 (9701, Cell Signaling Technology) at 1:1000; rabbit polyclonal anti-SOX2 (AB5603, EMD Millipore) at 1:200; rabbit polyclonal anti-SOX10 (GTX128374, GeneTex) at 1:200; rabbit polyclonal anti-OLIG2 (18953, IBL America) at 1:200; mouse monoclonal anti-HuC/HuD (A-21271, Invitrogen) at 1:300; rabbit polyclonal Living Colors DsRed (632496, Clonetech) at 1:200; rabbit anti-activated human caspase 3 (559565, BD Pharmingen) at 1:500.

Techniques: CRISPR, TALENs, Isolation, Immunolabeling, Expressing, RNA Sequencing Assay, Labeling

Differential gene expression of transcriptional regulators in rb1 tumor and rb1/rb1 mutant transcriptomes. (A) Comparative analysis of all differentially expressed transcriptional regulators in rb1 tumor and rb1/rb1 transcriptomes. (B) Heat maps of log2(FPKM) showing relative expression of components of the NuRD chromatin remodeler, neural progenitor and neurogenic transcription factors in rb1 tumor and rb1/rb1 mutant transcriptomes. Tables S3 and S6 contain fold change and P -values calculated using DESeq2. (C,D) Average fold change of rbbp4 , hdac1 , olig2 and ascl1b measured by qRT-PCR in triplicate (dark-gray bars) and transcriptome DESeq2 calculated values (light-gray bars) in rb1 tumor tissue versus normal adult brain (C) and 5dpf rb1/rb1 mutant versus wild-type larvae (D). metap1 , housekeeping gene used as a standard control for heat maps and qRT-PCR.

Journal: Disease Models & Mechanisms

Article Title: Epigenetic regulators Rbbp4 and Hdac1 are overexpressed in a zebrafish model of RB1 embryonal brain tumor, and are required for neural progenitor survival and proliferation

doi: 10.1242/dmm.034124

Figure Lengend Snippet: Differential gene expression of transcriptional regulators in rb1 tumor and rb1/rb1 mutant transcriptomes. (A) Comparative analysis of all differentially expressed transcriptional regulators in rb1 tumor and rb1/rb1 transcriptomes. (B) Heat maps of log2(FPKM) showing relative expression of components of the NuRD chromatin remodeler, neural progenitor and neurogenic transcription factors in rb1 tumor and rb1/rb1 mutant transcriptomes. Tables S3 and S6 contain fold change and P -values calculated using DESeq2. (C,D) Average fold change of rbbp4 , hdac1 , olig2 and ascl1b measured by qRT-PCR in triplicate (dark-gray bars) and transcriptome DESeq2 calculated values (light-gray bars) in rb1 tumor tissue versus normal adult brain (C) and 5dpf rb1/rb1 mutant versus wild-type larvae (D). metap1 , housekeeping gene used as a standard control for heat maps and qRT-PCR.

Article Snippet: Cryosections were labeled with the following antibodies: rabbit polyclonal anti-phosphohistone H3 (9701, Cell Signaling Technology) at 1:1000; rabbit polyclonal anti-SOX2 (AB5603, EMD Millipore) at 1:200; rabbit polyclonal anti-SOX10 (GTX128374, GeneTex) at 1:200; rabbit polyclonal anti-OLIG2 (18953, IBL America) at 1:200; mouse monoclonal anti-HuC/HuD (A-21271, Invitrogen) at 1:300; rabbit polyclonal Living Colors DsRed (632496, Clonetech) at 1:200; rabbit anti-activated human caspase 3 (559565, BD Pharmingen) at 1:500.

Techniques: Expressing, Mutagenesis, Quantitative RT-PCR