Rabbit Recombinant Monoclonal GLP-1 antibody. Carrier free. Suitable for WB, IHC-P, ELISA, ICC/IF and reacts with Human, Mouse, Rat, Synthetic peptide - Human samples.
pH: 7.2 - 7.4
Constituents: PBS
WB | IHC-P | ELISA | ICC/IF | |
---|---|---|---|---|
Human | Tested | Tested | Expected | Tested |
Mouse | Not recommended | Tested | Expected | Expected |
Rat | Not recommended | Tested | Expected | Expected |
Synthetic peptide - Human | Not recommended | Not recommended | Tested | Not recommended |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Rat, Mouse, Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info - | Notes - |
Species Rat | Dilution info - | Notes - |
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Glucagon. Plays a key role in glucose metabolism and homeostasis. Regulates blood glucose by increasing gluconeogenesis and decreasing glycolysis. A counterregulatory hormone of insulin, raises plasma glucose levels in response to insulin-induced hypoglycemia. Plays an important role in initiating and maintaining hyperglycemic conditions in diabetes. Glucagon-like peptide 1. Potent stimulator of glucose-dependent insulin release. Also stimulates insulin release in response to IL6 (PubMed:22037645). Plays important roles on gastric motility and the suppression of plasma glucagon levels. May be involved in the suppression of satiety and stimulation of glucose disposal in peripheral tissues, independent of the actions of insulin. Has growth-promoting activities on intestinal epithelium. May also regulate the hypothalamic pituitary axis (HPA) via effects on LH, TSH, CRH, oxytocin, and vasopressin secretion. Increases islet mass through stimulation of islet neogenesis and pancreatic beta cell proliferation. Inhibits beta cell apoptosis (Probable). Glucagon-like peptide 2. Stimulates intestinal growth and up-regulates villus height in the small intestine, concomitant with increased crypt cell proliferation and decreased enterocyte apoptosis. The gastrointestinal tract, from the stomach to the colon is the principal target for GLP-2 action. Plays a key role in nutrient homeostasis, enhancing nutrient assimilation through enhanced gastrointestinal function, as well as increasing nutrient disposal. Stimulates intestinal glucose transport and decreases mucosal permeability. Oxyntomodulin. Significantly reduces food intake. Inhibits gastric emptying in humans. Suppression of gastric emptying may lead to increased gastric distension, which may contribute to satiety by causing a sensation of fullness. Glicentin. May modulate gastric acid secretion and the gastro-pyloro-duodenal activity. May play an important role in intestinal mucosal growth in the early period of life.
Pro-glucagon, GCG
Rabbit Recombinant Monoclonal GLP-1 antibody. Carrier free. Suitable for WB, IHC-P, ELISA, ICC/IF and reacts with Human, Mouse, Rat, Synthetic peptide - Human samples.
pH: 7.2 - 7.4
Constituents: PBS
The mouse and rat recommendation is based on IHC-P result, we are not recommending WB in mouse and rat.
ab226036 is the carrier-free version of Anti-GLP-1 antibody [EPR4042-1] ab108443.
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
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:
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.
GLP-1 also known as glucagon-like peptide-1 is a 30 or 31 amino acid peptide with a mass of approximately 3.3 kDa. This peptide is mainly secreted by intestinal L-cells and the CNS. It enhances the secretion of insulin in response to glucose making it an important regulator of blood sugar levels. GLP-1 is degraded by dipeptidyl peptidase-4 which rapidly reduces its activity. Researchers often target GLP-1 in studies aimed at understanding metabolic processes and developing therapeutic interventions.
GLP-1 influences several physiological functions by acting on its receptor GLP-1R a G-protein coupled receptor. It is not part of a complex but exerts its effects through binding to this receptor. Activation of GLP-1R promotes insulin secretion suppresses glucagon release slows gastric emptying and promotes satiety. This makes GLP-1 an important regulator in energy homeostasis and nutrient absorption. Its effects on appetite and food intake are of particular interest in obesity research.
GLP-1 is an essential component of the incretin pathway which regulates insulin secretion in response to food intake. The interaction between GLP-1 and the GLP-1 receptor activates the adenylate cyclase pathway leading to increased cAMP and PKA signaling in pancreatic beta-cells. This chain of events enhances the insulin-secreting ability of these cells. Furthermore GLP-1 has connections with proteins such as insulin and glucagon through its regulatory functions in glucose metabolism.
GLP-1 is highly relevant to type 2 diabetes and obesity. Its ability to enhance insulin secretion and promote weight loss has made it a target for drug development in the treatment of these conditions. Antidiabetic medications including GLP-1 receptor agonists exploit this mechanism to control blood sugar levels effectively. Additionally GLP-1's connection to insulin makes it a significant focus in diabetes research as imbalances in these proteins contribute to the disease pathology.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.Unpurified Anti-GLP-1 antibody [EPR4042-1] ab108443, at 1/100 dilution, staining Glicentin in Human pancreas tissue by immunohistochemistry Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.1 ug/mL of Glucagon-like Peptide (GLP-1) was coated into 96-wells. Various concentrations of anti-Glucagon-Like Peptide 1 (GLP-1, 7-36,amide) rabbit monoclonal antibody (unpurified Anti-GLP-1 antibody [EPR4042-1] ab108443) was added. HRP conjugated goat anti-rabbit IgG antibody was used to develop the color.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.
Immunofluorescence staining of BxPC-3 cells with purified Anti-GLP-1 antibody [EPR4042-1] ab108443 at a working dilution of 1/800, counter-stained with DAPI. The secondary antibody was Alexa Fluor® 488 goat anti-rabbit (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077), used at a dilution of 1/1000. Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291, a mouse anti-tubulin antibody (1/1000), was used to stain tubulin along with Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (Alexa Fluor® 594 goat anti-mouse, 1/1000), shown in the top right hand panel. The cells were fixed in 4% PFA and permeabilized using 0.1% Triton X 100. The negative controls are shown in bottom middle and right hand panels - for negative control 1, purified Anti-GLP-1 antibody [EPR4042-1] ab108443 was used at a dilution of 1/500 followed by an Alexa Fluor® 594 goat anti-mouse antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at a dilution of 1/500. For negative control 2, Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (mouse anti-tubulin) was used at a dilution of 1/500 followed by an Alexa Fluor® 488 goat anti-rabbit antibody (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at a dilution of 1/400.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.Immunohistochemical staining of paraffin embedded human pancreas with purified Anti-GLP-1 antibody [EPR4042-1] ab108443 at a working dilution of 1/200. The secondary antibody used is HRP goat anti-rabbit IgG H&L (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-GLP-1 antibody [EPR4042-1] (Anti-GLP-1 antibody [EPR4042-1] ab108443) at 1/2000 dilution
All lanes: human fetal pancreas tissue lysate at 10 µg
All lanes: HRP goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 15 kDa, 21 kDa
Observed band size: 11 kDa
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.Immunohistochemical staining of paraffin embedded human liver with purified Anti-GLP-1 antibody [EPR4042-1] ab108443 at a working dilution of 1/200. The secondary antibody used is HRP goat anti-rabbit IgG H&L (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.Antigen dose-response curve using purified Anti-GLP-1 antibody [EPR4042-1] ab108443. Antibody concentration of 1 µg/mL. An Alkaline Phosphatase-conjugated goat anti-rabbit IgG (H+L) (1/2500) was used as the secondary antibody.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.Antibody dose-response curve using purified Anti-GLP-1 antibody [EPR4042-1] ab108443. Antigen concentration of 1 µg/mL. An Alkaline Phosphatase-conjugated goat anti-rabbit IgG (H+L) (1/2500) was used as the secondary antibody.
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-GLP-1 antibody [EPR4042-1] (Anti-GLP-1 antibody [EPR4042-1] ab108443) at 1/200 dilution
All lanes: GLP-1 peptide at 0.005 µg
Predicted band size: 21 kDa
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.
Immunohistochemistry analysis of paraffin-embedded sections of mouse pancreas tissue staining GLP-1 with Anti-GLP-1 antibody [EPR4042-1] ab108443 at 1/3000 dilution and ready-to-use secondary Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Counterstaining was done using Hematoxylin. Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 20 minutes.
Positive staining on islet of mouse pancreas.
The section was incubated with Anti-GLP-1 antibody [EPR4042-1] ab108443 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
This data was developed using Anti-GLP-1 antibody [EPR4042-1] ab108443, the same antibody clone in a different buffer formulation.
Immunohistochemistry analysis of paraffin-embedded sections of rat pancreas tissue staining GLP-1 with Anti-GLP-1 antibody [EPR4042-1] ab108443 at 1/3000 dilution and ready-to-use secondary Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Counterstaining was done using Hematoxylin. Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 20 minutes.
Positive staining on islet of rat pancreas.
The section was incubated with Anti-GLP-1 antibody [EPR4042-1] ab108443 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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