Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JE41-03 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 148 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human Caspr2 aa 1,284-1,331 / 1,331. |
Positive control: | Human brain tissue lysate, mouse brain tissue lysate, mouse hippocampus tissue lysate, rat hippocampus tissue lysate, rat brain tissue lysate, mouse cerebellum tissue lysate, human brain tissue, mouse brain tissue, rat brain tissue. |
Subcellular location: | Membrane. |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:200 |
Uniprot #: | SwissProt: Q9UHC6 Human | Q9CPW0 Mouse |
Alternative names: | AUTS15 CDFE Cell recognition molecule Caspr2 CNTNAP2 CNTP2 CNTP2_HUMAN Contactin-associated protein-like 2 Homolog of Drosophila neurexin IV NRXN4 PTHSL1 |
Fig1:
Western blot analysis of Caspr2 on different lysates with Rabbit anti-Caspr2 antibody (HA721598) at 1/1,000 dilution. Lane 1: Human brain tissue lysate Lane 2: Mouse brain tissue lysate Lane 3: Mouse hippocampus tissue lysate Lane 4: Rat hippocampus tissue lysate Lysates/proteins at 40 µg/Lane. Predicted band size: 148 kDa Observed band size: 150 kDa Exposure time: 5 minutes; 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 (HA721598) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Western blot analysis of Caspr2 on different lysates with Rabbit anti-Caspr2 antibody (HA721598) at 1/1,000 dilution. Lane 1: Rat brain tissue lysate Lane 2: Mouse cerebellum tissue lysate Lane 3: Mouse brain tissue lysate Lysates/proteins at 40 µg/Lane. Predicted band size: 148 kDa Observed band size: 150 kDa Exposure time: 2 minutes; 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 (HA721598) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature. |
Fig3:
Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-Caspr2 antibody (HA721598) 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 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721598) at 1/200 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. |
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Fig4:
Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-Caspr2 antibody (HA721598) 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 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721598) at 1/200 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. |
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Fig5:
Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-Caspr2 antibody (HA721598) 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 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721598) at 1/200 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. |