Recombinant Human Proinsulin Protein, CF

R&D Systems | Catalog # 1336-PN

R&D Systems
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Key Product Details

  • R&D Systems E. coli-derived Recombinant Human Proinsulin Protein (1336-PN)
  • Quality control testing to verify active proteins with lot specific assays by in-house scientists
  • All R&D Systems proteins are covered with a 100% guarantee

Source

E. coli

Accession Number

Applications

Bioactivity
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Product Specifications

Source

E. coli-derived human Proinsulin protein
Phe25-Asn110, with an N-terminal Met, 6-His tag and Lys

Purity

>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.

Endotoxin Level

<0.01 EU per 1 μg of the protein by the LAL method.

N-terminal Sequence Analysis

Met

Predicted Molecular Mass

10.5 kDa

SDS-PAGE

9 kDa, reducing conditions

Activity

Measured in a serum-free cell proliferation assay using MCF‑7 human breast cancer cells. Karey, K.P. et al. (1988) Cancer Research 48:4083.
The ED50 for this effect is 0.15-0.75 μg/mL.

Formulation, Preparation, and Storage

1336-PN
Formulation Lyophilized from a 0.2 μm filtered solution in PBS.
Reconstitution

Reconstitute at 100 μg/mL in sterile PBS.


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Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.

Calculators

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

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Background: Proinsulin

Proinsulin is synthesized as a single chain, 110 amino acid (aa) preproprecursor that contains a 24 aa signal sequence and an 86 aa proinsulin propeptide. Following removal of the signal peptide, the proinsulin peptide undergoes further proteolysis to generate mature insulin, a 51 aa disulfide-linked dimer that consists of a 30 aa B chain (aa 25 - 54) bound to a 21 aa A chain (aa 90 - 110). The 34 aa intervening peptide (aa 55 - 89) that connects the B and A chains is termed the C-peptide. Human proinsulin shares 84% and 80% aa sequence identity with rat and bovine proinsulin, respectively. Most of the sequence variation between species occurs in the region of the C-peptide (1). This peptide generates a structural conformation that allows for the correct formation of the intrachain disulphide bonds (1). Insulin is a molecule that facilitates the cellular uptake of glucose. This is accomplished by regulating the appearance of membrane glucose transporters. Low insulin levels or lack of insulin are associated with type 2 and type 1 diabetes mellitus, respectively. These conditions are associated with an increased risk for microvascular complications such as retinopathy, nephropathy, and peripheral neuropathy (3). Proinsulin also circulates, but its physiologic role is less well understood. It does possess about 25% of the activity of mature insulin, but it would seem unlikely to be a natural substitute for insulin (4). In type 2 diabetes, an elevated proinsulin to insulin ratio in the circulation is a well-known abnormality (5 - 9). Perhaps this abnormality represents either compromised proteolytic processing or a general inability to process increased levels of insulin precursor (5). In any event, proinsulin will stimulate amylin secretion by beta -cells, and amyloid formation in pancreatic islets that promotes decreased beta cell function (10). Studies also suggest that fasting serum proinsulin may be a better predictor of future type 2 diabetes than fasting insulin levels in obese children (11).

References

  1. Bell, G.I. et al. (1980) Nature 284:26.
  2. Barbetti, F. et al. (1990) J. Clin. Endocrinol. Metab. 71:164.
  3. Forst, T. et al. (2008) Exp. Diabetes Res. 2008:176245.
  4. Steffes, M.W. et al. (2003) Diabetes Care 26:832.
  5. Roder, M.E. et al. (1999) Diabetes Care 22:609.
  6. Porte, D. Jr. (1991) Diabetes 40:166.
  7. Gordon, P. et al. (1974) Diabetologia 34:483.
  8. Saad, M.F. et al. (1990) J. Clin. Endocrinol. Metab. 70:1247.
  9. Roder, M.E. et al. (1995) J. Clin. Endocrinol. Metab. 80:2359.
  10. Dworacka, M. et al. (2006) Int. J. Clin. Pharmacol. Ther. 44:14.
  11. Kamoda, T. et al. (2006) Diabetes Obes. Metab. 8:192.

Alternate Names

IDDM2, ILPR, insulin, IRDN, MODY10, proinsulin

Entrez Gene IDs

3630 (Human); 16333 (Mouse)

Gene Symbol

INS

Additional Proinsulin Products

Product Documents for Recombinant Human Proinsulin Protein, CF

Certificate of Analysis

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Note: Certificate of Analysis not available for kit components.

Product Specific Notices for Recombinant Human Proinsulin Protein, CF

For research use only

Citations for Recombinant Human Proinsulin Protein, CF

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FAQs

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Associated Pathways

Adipokines & Insulin Signaling Pathways Adipokines & Insulin Signaling Pathway Thumbnail