WB
Western blot analysis of Olig2 on different lysates with Rabbit anti-Olig2 antibody at 1/5,000 dilution. Lane 1: Mouse brain tissue lysate (20 µg/Lane), Lane 2: Rat brain tissue lysate (20 µg/Lane), Lane 3: Human brain tissue lysate (20 µg/Lane), Exposure time: 5 minutes 30 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.IHC
Immunohistochemical analysis of paraffin-embedded human glioma tissue with Rabbit anti-Olig2 antibody at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.IF-F
Immunofluorescence analysis of frozen E14.5 mouse embryonic brain tissue with Rabbit anti-Olig2 antibody at 1/500 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (green) at 1/500 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).IF-P
Immunofluorescence analysis of paraffin-embedded mouse hippocampus tissue labeling Olig2 with Rabbit anti-Olig2 antibody at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).| Product Name | Olig2 Recombinant Rabbit Monoclonal Antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Immunogen | Synthetic peptide within Human Olig2 aa 238-287 / 323. |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | IF-FIF-PIHCWB |
| WB:1:5000 IHC:1:1000 IF-F:1:500 IF-P:1:200 |
|
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Purification | Protein A |
| Gene Symbol | OLIG2 |
|---|---|
| Gene Synonyms | BHLHB1 OLIGO2 RACK17 PRKCBP2 bHLHe19 |
| Gene Full Name | oligodendrocyte transcription factor 2 |
| Gene Summary | This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14;21)(q11.2;q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome. [provided by RefSeq, Jul 2008] |
| Alternative Names | Basic domain helix loop helix protein class B 1 antibody Basic helix loop helix protein class B 1 antibody BHLHB antibody bHLHB1 antibody bHLHe19 antibody Class B basic helix loop helix protein 1 antibody Class B basic helix-loop-helix protein 1 antibody class E basic helix loop helix protein 19 antibody Class E basic helix-loop-helix protein 19 antibody Human protein kinase C binding protein RACK17 antibody Basic domain helix loop helix protein class B 1 antibody Basic helix loop helix protein class B 1 antibody BHLHB antibody bHLHB1 antibody bHLHe19 antibody Class B basic helix loop helix protein 1 antibody Class B basic helix-loop-helix protein 1 antibody class E basic helix loop helix protein 19 antibody Class E basic helix-loop-helix protein 19 antibody Human protein kinase C binding protein RACK17 antibody Olig2 antibody OLIG2_HUMAN antibody Oligo2 antibody Oligodendrocyte lineage transcription factor 2 antibody Oligodendrocyte specific bHLH transcription factor 2 antibody Oligodendrocyte transcription factor 2 antibody OTTHUMP00000067569 antibody OTTHUMP00000067570 antibody PRKCBP2 antibody Protein kinase C binding protein 2 antibody Protein kinase C binding protein RACK17 antibody Protein kinase C-binding protein 2 antibody Protein kinase C-binding protein RACK17 antibody RACK17 antibody |
| Molecular Weight(MW) | 32kDa(Observed band size: 36kDa) |
| Cellular Localization | Nucleus, Cytoplasm. |
WB
Western blot analysis of Olig2 on different lysates with Rabbit anti-Olig2 antibody at 1/5,000 dilution. Lane 1: Mouse brain tissue lysate (20 µg/Lane), Lane 2: Rat brain tissue lysate (20 µg/Lane), Lane 3: Human brain tissue lysate (20 µg/Lane), Exposure time: 5 minutes 30 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.
IHC
Immunohistochemical analysis of paraffin-embedded human glioma tissue with Rabbit anti-Olig2 antibody at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
IF-F
Immunofluorescence analysis of frozen E14.5 mouse embryonic brain tissue with Rabbit anti-Olig2 antibody at 1/500 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (green) at 1/500 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
IF-P
Immunofluorescence analysis of paraffin-embedded mouse hippocampus tissue labeling Olig2 with Rabbit anti-Olig2 antibody at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).| Application Notes | WB:1:5000 IHC:1:1000 IF-F:1:500 IF-P:1:200 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
