Mouse Insulin ELISA - 10 Pack

Mouse Insulin ELISA – 10 Pack

(10-1247-10)

Kit format: 1 x 96 wells

Measurement range: 0.2 - 6.5 µg/L

Bulk volumes suitable for large quantities of samples

Low sample volume - 10 μL (5 µL assay protocol available)

Insignificant or no cross reactivity to C-peptide or proinsulin

Controls available: 10-1220-01

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Description

The Mercodia Mouse Insulin ELISA is an easy-to-use assay based on highly specific monoclonal antibodies with insignificant or no cross-reactivity to C-peptide or proinsulin.

Please note that the 10 pack Mercodia Mouse Insulin ELISA is delivered in bulk and is suitable if you run larger quantities of samples.

Test characteristics

Species

Mouse

Sample type

Serum, EDTA plasma and cell culture medium

Sample volume

10 µL (5 µL protocol available)

Assay range

0.2 - 6.5 µg/L

Detection limit

≤ 0.2 µg/L

Incubation

2 h + 15 min

specificity

The following cross-reactions have been tested:

The Mercodia Mouse Insulin ELISA is an easy-to-use assay based on highly specific monoclonal antibodies with insignificant or no cross-reactivity to C-peptide or proinsulin.

Mouse C-peptide I

Not detected

Mouse C-peptide II

Not detected

Rat C-peptide I

Not detected

Rat C-peptide II

Not detected

Rat insulin

146 %

Mouse proinsulin I

43 %

Mouse proinsulin II

60 %

Rat proinsulin I

14 %

Rat proinsulin II

60 %

Human insulin

195 %

Human proinsulin

82 %

Human C-peptide

Not detected

directions for use & Safety Data Sheet

Directions for Use - 10-1247-10 Version 9.0 Lot.no 35394, 35609

Safety Data Sheet - 10-1247-10

For other languages and older versions:

Technical Library

technical notes

For product-specific technical notes see:
TN34-0130 5µL sample volume in Mercodia’s Mouse Insulin and Rat Insulin ELISAs

references

Fischer, C. et al. (2017). A miR-327-FGF10-FGFR2-mediated autocrine signaling mechanism controls white fat browning. Nature Communications, 8(1), 2079. Read more >

Kleiner, S. et al. (2018). Mice harboring the human SLC30A8 R138X loss-of-function mutation have increased insulin secretory capacity. Proceedings of the National Academy of Sciences of the United States of America, 115(32), E7642–E7649. Read more >

Ikeda, Y. et al. (2018). Glucagon and/or IGF-1 Production Regulates Resetting of the Liver Circadian Clock in Response to a Protein or Amino Acid-only Diet. EBioMedicine, pp. 210–224. Read more >

Figueiredo, H. et al. (2019). Targeting pancreatic islet PTP1B improves islet graft revascularization and transplant outcomes. Science Translational Medicine, 11(497), eaar6294. Read more >

Aarts, S., Reiche, M., den Toom, M., Gijbels, M., Beckers, L., Gerdes, N., & Lutgens, E. (2019). Depletion of CD40 on CD11c+ cells worsens the metabolic syndrome and ameliorates hepatic inflammation during NASH. Scientific Reports, 9(1), 14702. Read more >