NeuroD1 Recombinant Rabbit Monoclonal Antibody [JM11-10]
cat.: ET1703-73
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human, Mouse, Rat, Cynomolgus monkey, Pig |
| Applications: | WB, IP, IHC-P, IHC-Fr |
| Clonality: | Monoclonal |
| Clone number: | JM11-10 |
| Form: | Liquid |
| Storage condition: | 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. |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 40 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide within Human NeuroD1 aa 1-44 / 356. |
| Positive control: | Mouse cerebellum tissue, rat brain tissue, rat cerebellum tissue, Mouse cerebellum (P7) tissue lysate, Mouse cerebellum tissue lysate, Rat cerebellum tissue lysate. |
| Subcellular location: | Cytoplasm. Nucleus. |
| Recommended Dilutions:
WB IP IHC-P IHC-Fr |
1:1,000 1:10-1:50 1:200-1:500 1:100 |
| Uniprot #: | SwissProt: Q13562 Human | Q60867 Mouse | Q64289 Rat |
| Alternative names: | atonal basic helix loop helix transcription factor BETA 2 Beta cell E box transactivator 2 BETA2 BHF 1 BHF1 bHLHa3 class A basic helix loop helix protein 3 Class A basic helix-loop-helix protein 3 MODY 6 MODY6 NDF1_HUMAN NeuroD NeuroD1 Neurogenic differentiation 1 Neurogenic differentiation factor 1 neurogenic helix loop helix protein NEUROD Neuronal differentiation 1 |
Images
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Fig1:
Application: IHC-Fr Species: Mouse Site: Cerebellum Sample: Frozen section Antibody concentration: 1:100 Antigen retrieval: Recommend. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. |
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Fig2:
Application: IHC-Fr Species: Rat Site: Cerebellum Sample: Frozen section Antibody concentration: 1:100 Antigen retrieval: Recommend. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. |
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Fig3:
Western blot analysis of NeuroD1 on different lysates with Rabbit anti-NeuroD1 antibody (ET1703-73) at 1/1,000 dilution. Lane 1: Mouse cerebellum (P7) tissue lysate (40 µg/Lane) Lane 2: Mouse cerebellum tissue lysate (no heat) (40 µg/Lane) Lane 3: Mouse liver tissue lysate (negative) (40 µg/Lane) Lane 4: Rat cerebellum tissue lysate (40 µg/Lane) Lane 5: Rat liver tissue lysate (negative) (40 µg/Lane) Notice: no heat means the lysate is not boiled. Predicted band size: 40 kDa Observed band size: 50 kDa Exposure time: 51 seconds; ECL: K1801; 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 (ET1703-73) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig4:
Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue with Rabbit anti-NeuroD1 antibody (ET1703-73) at 1/500 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 (ET1703-73) at 1/500 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-NeuroD1 antibody (ET1703-73) at 1/400 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 (ET1703-73) at 1/400 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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Fig6:
Immunohistochemical analysis of paraffin-embedded rat cerebellum tissue with Rabbit anti-NeuroD1 antibody (ET1703-73) at 1/200 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 (ET1703-73) 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. |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.