Anti-VGF antibody [EPR27029-73] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- Advanced Validation
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Rabbit Recombinant Monoclonal VGF antibody. Carrier free. Suitable for WB, IHC-P, mIHC and reacts with Human, Mouse, Rat samples.
View Alternative Names
Neurosecretory protein VGF, VGF
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human adrenal gland tissue labelling VGF with ab308287 at 1/500 (1.033 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human adrenal medulla. The section was incubated with ab308287 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human pituitary glan tissue labelling VGF with ab308287 at 1/500 (1.033 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human pituitary gland. The section was incubated with ab308287 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human kidney tissue labelling VGF with ab308287 at 1/500 (1.033 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on human kidney. The section was incubated with ab308287 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat adrenal gland tissue labelling VGF with ab308287 at 1/500 (1.033 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on rat adrenal medulla. The section was incubated with ab308287 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- mIHC
Lab
Multiplex immunohistochemistry - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Mouse adrenal gland staining of ADX with ab321899 at a 1/2000 (0.244 µg/ml) dilution, VGF with ab308287 at 1/500 (0.95 µg/ml) dilution and Neuropeptide Y with ab221145 at 1/4000 ( 0.140 µg/ml) dilution.
Panel A : merged staining of anti-ADX (gray; Opal™690), anti-VGF (green; Opal™520) and anti-Neuropeptide Y (magenta; Opal™570) on mouse adrenal gland.
Panel B : anti-ADX staining adrenal cortex in mouse adrenal gland.
Panel C : anti-VGF staining endocrine cells in mouse adrenal gland medulla.
Panel D : nti-Neuropeptide Y staining chromaffin cells in mouse adrenal gland medulla.
Nuclear DNA was labelled with DAPI (shown in blue). ).
The section was incubated in three rounds of staining : in the order of ab321899, ab308287 and ab221145 for 30 mins at room temperature.. Each round was followed by a separate fluorescent tyramide signal amplification system.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0 epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat pituitary gland tissue labelling VGF with ab308287 at 1/500 (1.033 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on rat pituitary gland. The section was incubated with ab308287 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
Immunohistochemical analysis of paraffin-embedded Mouse adrenal gland tissue labelling VGF with ab308287 at 1/500 (1.033 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse adrenal medulla. The section was incubated with ab308287 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Supplier Data
Western blot - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using ab308287, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. The primary band at 90 kDa is the precursor form of VGF which is consistent with literature descriptions (PMID : 30690892, PMID : 10433233). In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-VGF antibody [EPR27029-73] (<a href='/en-us/products/primary-antibodies/vgf-antibody-epr27029-73-ab308287'>ab308287</a>) at 1/1000 dilution
Lane 1:
Untreated U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
U-2 OS treated with /ml BFA for 24 hour whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 67 kDa
Observed band size: 90 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using 308287, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. The primary band at 90 kDa is the precursor form of VGF which is consistent with literature descriptions (PMID : 30690892, PMID : 10433233). In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-VGF antibody [EPR27029-73] (<a href='/en-us/products/primary-antibodies/vgf-antibody-epr27029-73-ab308287'>ab308287</a>) at 1/1000 dilution
Lane 1:
Untreated PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate at 20 µg
Lane 2:
PC-12 treated with /ml BFA for 24 hour whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 67 kDa
Observed band size: 90 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-VGF antibody [EPR27029-73] - BSA and Azide free (AB308290)
This data was developed using 308287, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Negative control : RAW 264.7. The identities of the lower MW bands between 37 kDa and 90 kDa are expected to be VGF peptides. The primary band at 90 kDa is the precursor form of VGF which is consistent with literature descriptions (PMID : 30690892, PMID : 10433233). Lysates were freshly made and used for Western blotting immediately to minimize protein degradation. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-VGF antibody [EPR27029-73] (<a href='/en-us/products/primary-antibodies/vgf-antibody-epr27029-73-ab308287'>ab308287</a>) at 1/1000 dilution
Lane 1:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 2:
RAW264.7 (mouse elson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 67 kDa
Observed band size: 90 kDa
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-VGF antibody [EPR27029-73]
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
VGF-derived peptides exert significant influence on energy balance neurogenesis and synaptic plasticity. These peptides participate in the regulation of appetite and energy expenditure contributing to body weight management. They are also involved in nerve growth and repair mechanisms. VGF peptides act independently or in conjunction with other neuropeptides and factors within the nervous system though it does not form a stable complex with other proteins.
Pathways
Few proteins have as diverse involvement as VGF in the neuroendocrine system's regulation. VGF links to the neurotrophic signaling pathway which promotes neuronal survival and growth. It shows interactions with proteins such as Brain-Derived Neurotrophic Factor (BDNF) and Nerve Growth Factor (NGF) which support cellular health and energy homeostasis. VGF's role assists in the modulation of these pathways facilitating communication between energy state signals and neuronal networks.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com