![Western Blot: GAP-43 Antibody [NB100-81934] - Analysis of extract from mouse brain tissue, using NB100-81934 and the same antibody preincubated with blocking peptide.](http://images.novusbio.com/fullsize/GAP-43-Antibody-Western-Blot-NB100-81934-img0006.jpg "Western Blot: GAP-43 Antibody [NB100-81934] - Analysis of extract from mouse brain tissue, using NB100-81934 and the same antibody preincubated with blocking peptide.")
| Reactivity | Hu, Mu, RtSpecies Glossary |
| Applications | WB, ICC/IF, IHC |
| Clonality | Polyclonal |
| Host | Rabbit |
| Conjugate | Unconjugated |
| Concentration | 1.0 mg/ml |
| Immunogen | The antiserum was produced against synthesized non-phosphopeptide derived from human GAP-43 around amino acids 38~43 (Q-A-S-F-R). |
| Marker | Neuronal Marker |
| Specificity | Detects endogenous levels of total GAP-43 protein. |
| Isotype | IgG |
| Clonality | Polyclonal |
| Host | Rabbit |
| Gene | GAP43 |
| Purity | Immunogen affinity purified |
| Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. |
| Dilutions |
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| Theoretical MW | 43 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
| Storage | Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles. |
| Buffer | PBS (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 50% glycerol |
| Preservative | 0.02% Sodium Azide |
| Concentration | 1.0 mg/ml |
| Purity | Immunogen affinity purified |
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Secondary Antibodies |
Isotype Controls |
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![Immunocytochemistry/ Immunofluorescence: GAP-43 Antibody [NB100-81934] - Staining of methanol-fixed Hela cells using NB100-81934](http://images.novusbio.com/fullsize/GAP-43-Antibody-Immunocytochemistry-Immunofluorescence-NB100-81934-img0004.jpg "Immunocytochemistry/ Immunofluorescence: GAP-43 Antibody [NB100-81934] - Staining of methanol-fixed Hela cells using NB100-81934")
![Immunohistochemistry-Paraffin: GAP-43 Antibody [NB100-81934] - Analysis of paraffin-embedded human breast carcinoma tissue, using NB100-81934 (left) or the same antibody preincubated with blocking peptide (right).](http://images.novusbio.com/fullsize/GAP-43-Antibody-Immunohistochemistry-NB100-81934-img0005.jpg "Immunohistochemistry-Paraffin: GAP-43 Antibody [NB100-81934] - Analysis of paraffin-embedded human breast carcinoma tissue, using NB100-81934 (left) or the same antibody preincubated with blocking peptide (right).")
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![Western Blot: Goat anti-Rabbit IgG (H+L) Secondary Antibody [HRP] [NB7160] - Western blot showing vemurafenib treatment in BRAFV600E CRC cells inhibits fission mediator DRP1 with no significant effect on fusion proteins (Mfn1 & 2) using MFN-1 antibody (NBP1-51841) and corresponding secondary antibody, goat anti-rabbit IgG-HRP (NB7160). Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33738242).](https://images.novusbio.com/images/Goat-anti-Rabbit-IgG-H+L-Secondary-Antibody-HRP-Western-Blot-NB7160-img0001.jpg "Western Blot: Goat anti-Rabbit IgG (H+L) Secondary Antibody [HRP] [NB7160] - Western blot showing vemurafenib treatment in BRAFV600E CRC cells inhibits fission mediator DRP1 with no significant effect on fusion proteins (Mfn1 & 2) using MFN-1 antibody (NBP1-51841) and corresponding secondary antibody, goat anti-rabbit IgG-HRP (NB7160). Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33738242).")
![Flow Cytometry: Rabbit IgG Isotype Control [NBP2-24891] - Intracellular FACS analysis of mouse TLR6 polyclonal antibody (red), rabbit isotype control (green), RAW cells alone (shaded). Two micrograms of antibodies were used. Goat anti-rabbit FITC (Novus, 20302) was used as secondary.](https://images.novusbio.com/images/Rabbit--Mouse-IgG-Isotype-Control-Flow-Cytometry-NBP2-24891-img0001.jpg "Flow Cytometry: Rabbit IgG Isotype Control [NBP2-24891] - Intracellular FACS analysis of mouse TLR6 polyclonal antibody (red), rabbit isotype control (green), RAW cells alone (shaded). Two micrograms of antibodies were used. Goat anti-rabbit FITC (Novus, 20302) was used as secondary.")