Western Blot Antibodies are antibodies for immunoblotting applications, capable of recognizing linear epitopes under denaturing conditions to enable qualitative and semi-quantitative analysis of target proteins. Key experimental steps include blocking (5% non-fat milk or BSA to minimize non-specific binding), antibody dilution (primary antibody typically 1:1000–1:10000 for optimal signal-to-noise ratio), thorough washing (TBST to remove unbound antibodies), matched secondary antibody (HRP- or fluorophore-conjugated, species-specific), and loading control normalization (β-actin, GAPDH, etc.). Primary applications encompass protein expression analysis (validation of overexpression or knockdown efficiency), post-translational modification detection (phosphorylation, acetylation status), protein-protein interaction verification (detection of co-immunoprecipitated proteins), biomarker screening (differential expression of disease-associated proteins), and antibody quality control, serving as fundamental tools in molecular biology and protein research.
INSR is a receptor that binds insulin and has a tyrosine-protein kinase activity. Autophosphorylation activates the kinase activity. This Type I mebrane protein is composed of a tetramer of 2 alpha and 2 beta chains linked by disulfide bonds. The alpha chains contribute to the formation of the ligand-binding domain, while the beta chains carry the kinase domain. After being transported from the endoplasmic reticulum to the Golgi apparatus, the single glycosylated precursor is further glycosylated and then cleaved, followed by its transport to the plasma membrane. Defects in INSR are the cause of insulin resistance of various forms, including mild insulin-resistant diabetes mellitus with acanthosis nigricans, minor physical abnormalities and sometimes polycystic ovaries. Insulin resistance associated with acanthosis nigricans, hirsutism and hyperandrogenism is referred to as insulin resistance type A. Defects in INSR are the cause of Rabson-Mendenhall syndrome, also known as Mendenhall syndrome. It is a severe insulin resistance syndrome characterized by insulin-resistant diabetes mellitus with pineal hyperplasia and somatic abnormalities. Typical features include coarse, senile-appearing facies, dental and skin abnormalities, abdominal distension, and phallic enlargement. Inheritance is autosomal recessive. Defects in INSR are the cause of leprechaunism, also known as Donohue syndrome. Leprechaunism represents the most severe form of insulin resistance syndrome, characterized by intrauterine and postnatal growth retardation and death in early infancy. Inheritance is autosomal recessive. Defects in INSR may be associated with noninsulin-dependent diabetes mellitus.
This product is currently in development. The lead time for this product may be several months. Please contact us at [email protected] for an updated lead time before purchasing this product. Fatty Acid Transport Protein 1 (FATP1) Antibody is a Mouse Monoclonal antibody against Fatty Acid Transport Protein 1 (FATP1).
This product is currently in development. The lead time for this product may be several months. Please contact us at [email protected] for an updated lead time before purchasing this product. Excitatory Amino Acid Transporter 4 (EAAT4) Antibody is a Mouse Monoclonal antibody against Excitatory Amino Acid Transporter 4 (EAAT4).