Rabbit Polyclonal Anti-Insulin antibody (STJ98980)


Reactivity: Human, Mouse, Rat
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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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

Image descriptions:

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Alternative names:

Check alternative names for the antibody


|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|


Anti-Insulin antibody

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.


1 mg/ml


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

Primary antibody


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