MAb to Insulin | MyBioSource MBS310703 product information

product summary

request information :

company name :

MyBioSource

product type :

antibody

product name :

MAb to Insulin

catalog :

MBS310703

quantity :

1 mg

price :

465 USD

clonality :

monoclonal

host :

mouse

reactivity :

human

application :

enzyme immunoassay, ELISA, radioimmunoassay

more info or order :

MyBioSource product webpage

product information

catalog number :

MBS310703

products type :

Antibody

products full name :

MAb to Insulin

products short name :

Insulin

products name syn :

Monoclonal Antibody to Human Insulin

other names :

insulin; Insulin; insulin; proinsulin; OTTHUMP00000011161; OTTHUMP00000011162; OTTHUMP00000196036; OTTHUMP00000196038; OTTHUMP00000217519; insulin; N/A

other gene names :

INS; INS; ILPR; IRDN; IDDM2; MODY10; N/A

uniprot entry name :

INS_HUMAN

clonality :

Monoclonal

isotype :

IgG1, kappa

clone :

D4B8

host :

Mouse. Hybridization of X63-Ag8-653 myeloma cells with spleen cells from BALB/c mice.

sequence length :

110

specificity :

Insulin. Insulin, human. Cross-reacts with human proinsulin, bovine insulin (30%) and porcine insulin. Does not react with free C-peptide.

purity :

>90% pure. Protein A chromatography

form :

Purified, Liquid

concentration :

4.1mg/ml (OD280nm, E^0.1% = 1.4)

storage stability :

Store at 2 to 8 degree C.

tested application :

EIA/ELISA, Immunohistochemistry - Formalin, Immunoassay Antibody Pairs, Radioimmunoassay

app notes :

Detection of insulin of two-site enzyme immunoassay. May be used in immunohistochemistry on frozen sections. Each laboratory should determine an optimum working titer for use in its particular application. Other applications have not been tested but use i

other info1 :

Immunogen: Purified human insulin. Affinity Constant: Kass=1.5 x 10^8 M^-1

other info2 :

Buffer: PBS, pH 7.4. Preservative: 0.1% Sodium azide. Important Note: Centrifuge before opening to ensure complete recovery of vial contents. Warnings: This product contains sodium azide, which has been classified as Xn (Harmful), in European Directive 67/548/EEC in the concentration range of 0.1-1.0%. When disposing of this reagent through lead or copper plumbing, flush with copious volumes of water to prevent azide build-up in drains.

products categories :

Monoclonal Antibodies to Hormones and Steroids

ncbi gi num :

386828

ncbi acc num :

AAA59172.1

uniprot acc num :

P01308

ncbi mol weight :

11,981 Da

ncbi pathways :

ATF-2 Transcription Factor Network Pathway 138006!!Adipogenesis Pathway 198832!!Aldosterone-regulated Sodium Reabsorption Pathway 130626!!Aldosterone-regulated Sodium Reabsorption Pathway 130590!!Amyloids Pathway 366238!!Arf6 Trafficking Events Pathway 137954!!Diabetes Pathways 105902!!Downstream Signaling Of Activated FGFR Pathway 160957!!FOXA1 Transcription Factor Network Pathway 137979!!FOXA2 And FOXA3 Transcription Factor Networks Pathway 137911

ncbi summary :

After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form insulin, and C-peptide. Binding of insulin to the insulin receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region. Alternative splicing results in multiple transcript variants. [provided by RefSeq]

uniprot summary :

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. Subunit structure: Heterodimer of a B chain and an A chain linked by two disulfide bonds. Subcellular location: Secreted. Involvement in disease: Defects in INS are the cause of familial hyperproinsulinemia (FHPRI) [. MIM:176730]. Ref.21 Ref.23 Ref.24 Ref.25Defects in INS are a cause of diabetes mellitus insulin-dependent type 2 (IDDM2) [. MIM:125852]. IDDM2 is a multifactorial disorder of glucose homeostasis that is characterized by susceptibility to ketoacidosis in the absence of insulin therapy. Clinical fetaures 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. Ref.34Defects in INS are a cause of diabetes mellitus permanent neonatal (PNDM) [. MIM:606176]. PNDM is 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. Ref.32 Ref.33Defects in INS are a cause of maturity-onset diabetes of the young type 10 (MODY10) [. MIM:613370]. MODY10 is 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. Ref.33 Ref.34 Ref.35. Pharmaceutical use: Available under the names Humulin or Humalog (Eli Lilly) and Novolin (Novo Nordisk). Used in the treatment of diabetes. Humalog is an insulin analog with 52-Lys-Pro-53 instead of 52-Pro-Lys-53. Sequence similarities: Belongs to the insulin family. Sequence caution: The sequence AAA59179.1 differs from that shown. Reason: Erroneous gene model prediction.

size :

1 mg

price :

465 USD

more info or order :

MyBioSource product webpage