Gastric Inhibitory Polypeptide (GIP) Antibody (FITC)

260€ (50 µl)
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935106861
info@markelab.com
name
Gastric Inhibitory Polypeptide (GIP) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx341969
Description
Gastric Inhibitory Polypeptide (GIP) Antibody (FITC) is a Rabbit Polyclonal antibody conjugated to FITC for the detection of Human GIP.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Gastric Inhibitory Polypeptide (GIP) |
Host | Rabbit |
Reactivity | Human |
Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | FITC |
Isotype | IgG |
Purity | > 95% |
Purification | Purified by Protein G chromatography. |
Size 1 | 50 µl |
Size 2 | 100 µl |
Size 3 | 200 µl |
Size 4 | 1 ml |
Form | Liquid |
Buffer | 0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P09681 |
Gene ID | 2695 |
Alias | Glucose-dependent insulinotropic polypeptide,Incretin |
Background | Antibody anti-GIP |
Status | RUO |
Descripción
GIP, also called glucose-dependent insulinotropic polypeptide, is a 42-amino acid hormone secreted by K-cells in the duodenum and jejunum in response to nutrient ingestion, particularly glucose, fats, and amino acids GIP acts as a critical incretin hormone that enhances glucose-dependent insulin secretion from pancreatic β-cells by activating cAMP-dependent pathways and protein kinase A signaling GIP also regulates lipid metabolism by stimulating lipoprotein lipase activity in adipose tissue, promoting triglyceride uptake and energy storage GIP further supports bone homeostasis by enhancing osteoblast function, contributing to bone formation and mineralization Dysregulation of GIP levels and signaling is associated with insulin resistance, obesity, and type 2 diabetes where its insulinotropic effects are impaired despite elevated circulating levels GIP-based therapies, including dual GIP/GLP-1 receptor agonists, have shown therapeutic potential in improving glycemic control and promoting weight loss in metabolic disorders
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