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KD-Validated Growth Associated Protein 43 Recombinant Rabbit mAb

#63163

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using Growth associated protein 43 antibody (Cat#63163). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using growth associated protein 43 antibody (Cat#63163). Growth associated protein 43 expression in wild type (WT) and growth associated protein 43 (GAP43) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunohistochemistry was performed on paraffin-embedded human glioblastoma using growth associated protein 43 antibody (Cat#63163, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HAP-1 cells with Growth associated protein 43 antibody (Cat#63163, 1:1,000). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Immunocytochemical staining of HeLa cells using growth associated protein 43 antibody (Cat#63163, 1:1,000), Top panel: wild-type (WT); Bottom panal: growth associated protein 43 shRNA knockdown (KD). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of growth associated protein 43 expression in HAP-1 cells using growth associated protein 43 antibody (Cat#63163, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, growth associated protein 43.
Validation of Growth associated protein 43 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with Growth associated protein 43 antibody (Cat#63163, 1:2,000) and analyzed using CytoFLEX. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use.
Please select the specifications of the product.
Specification:
Unit price:
$89.00
Quantity:
1
(Excluding sales tax)
  • Gene Symbol:
    GAP43
  • Catalog:
    63163
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H
Information
Product Name KD-Validated Growth Associated Protein 43 Recombinant Rabbit mAb
Aliases GAP43; Growth Associated Protein 43; Axonal Membrane Protein GAP-43; Neural Phosphoprotein B-50; Neuromodulin; GAP-43; B-50; PP46; Neuron Growth-Associated Protein 43; Nerve Growth-Related Peptide GAP43; Calmodulin-Binding Protein P-57; Protein F1; Growth-Associated Protein 43; Pp46
Background

Gene Name: GAP43

NCBI Gene Entry: 2596

UniProt Entry: P17677

Application Information

Molecular Weight: Predicted, 25 kDa; observed, 48 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB1195

Species Reactivity: Human

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC), immunohistochemistry-paraffin (IHC-P)

Immunogen A synthesized peptide derived from human GAP43
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:1,000-1:50,000
Flow Cytometry (FCM): 1:200-1:2,000
Immunocytochemistry (ICC): 1:100-1:1,000
Immunohistochemistry-Paraffin (IHC-P): 1:100-1:200
Note This product is for research use only.
Data
  • Western blotting analysis using Growth associated protein 43 antibody (Cat#63163). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using growth associated protein 43 antibody (Cat#63163). Growth associated protein 43 expression in wild type (WT) and growth associated protein 43 (GAP43) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Immunohistochemistry was performed on paraffin-embedded human glioblastoma using growth associated protein 43 antibody (Cat#63163, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • Immunocytochemical staining of HAP-1 cells with Growth associated protein 43 antibody (Cat#63163, 1:1,000). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
  • Immunocytochemical staining of HeLa cells using growth associated protein 43 antibody (Cat#63163, 1:1,000), Top panel: wild-type (WT); Bottom panal: growth associated protein 43 shRNA knockdown (KD). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
  • Flow cytometric analysis of growth associated protein 43 expression in HAP-1 cells using growth associated protein 43 antibody (Cat#63163, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, growth associated protein 43.
  • Validation of Growth associated protein 43 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with Growth associated protein 43 antibody (Cat#63163, 1:2,000) and analyzed using CytoFLEX. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use.
Western blotting analysis using Growth associated protein 43 antibody (Cat#63163). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using growth associated protein 43 antibody (Cat#63163). Growth associated protein 43 expression in wild type (WT) and growth associated protein 43 (GAP43) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunohistochemistry was performed on paraffin-embedded human glioblastoma using growth associated protein 43 antibody (Cat#63163, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HAP-1 cells with Growth associated protein 43 antibody (Cat#63163, 1:1,000). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Immunocytochemical staining of HeLa cells using growth associated protein 43 antibody (Cat#63163, 1:1,000), Top panel: wild-type (WT); Bottom panal: growth associated protein 43 shRNA knockdown (KD). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of growth associated protein 43 expression in HAP-1 cells using growth associated protein 43 antibody (Cat#63163, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, growth associated protein 43.
Validation of Growth associated protein 43 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with Growth associated protein 43 antibody (Cat#63163, 1:2,000) and analyzed using CytoFLEX. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use.
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