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Rabbit Polyclonal Anti-Insulin antibody (STJ98980)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000
Recommended protocols: check protocols
Click or hover above images to see image description for Anti-Insulin antibody.
Check alternative names for the antibodyExpand
|IDDM antibody|IDDM1 antibody|IDDM2 antibody|ILPR antibody|ins antibody|INS_HUMAN antibody|Insulin A chain antibody|Insulin B chain antibody|IRDN antibody|MODY10 antibody|Preproinsulin antibody|Proinsulin antibody|Proinsulin precursor antibody|Anti-Insulin antibody (ab7842)
SCBT cat No: sc-7839|sc-26795|sc-52033|sc-52034|sc-8033|sc-52035|sc-52036|sc-52037|sc-51647|sc-9168|sc-377071|sc-7838|
|Catalogue No.|| |
Human, Mouse, Rat
Anti-Insulin antibody detects endogenous Insulin .
Synthetic peptide from human protein at AA range: 30-70.
|Recommended dilution|| |
WB 1:500-2000; ELISA 1:10000-20000
Anti-Insulin antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Anti-Insulin antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
IDDM antibody, IDDM1 antibody, IDDM2 antibody, ILPR antibody, ins antibody, INS_HUMAN antibody, Insulin A chain antibody, Insulin B chain antibody, IRDN antibody, MODY10 antibody, Preproinsulin antibody, Proinsulin antibody, Proinsulin precursor antibody
|Database links|| |
|Protein function|| |
Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver.
|Involvement in disease|| |
Hyperproinsulinemia (HPRI) [MIM:616214]: An autosomal dominant condition characterized by elevated levels of serum proinsulin-like material. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Diabetes mellitus, insulin-dependent, 2 (IDDM2) [MIM:125852]: A multifactorial disorder of glucose homeostasis that is characterized by susceptibility to ketoacidosis in the absence of insulin therapy. Clinical features are polydipsia, polyphagia and polyuria which result from hyperglycemia-induced osmotic diuresis and secondary thirst. These derangements result in long-term complications that affect the eyes, kidneys, nerves, and blood vessels. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176]: A rare form of diabetes distinct from childhood-onset autoimmune diabetes mellitus type 1. It is characterized by insulin-requiring hyperglycemia that is diagnosed within the first months of life. Permanent neonatal diabetes requires lifelong therapy. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Maturity-onset diabetes of the young 10 (MODY10) [MIM:613370]: A form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age), a primary defect in insulin secretion and frequent insulin-independence at the beginning of the disease. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the insulin family.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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