EZRMCP2

Rat/Mouse C-Peptide 2 ELISA Kit

Name: Rat/Mouse C-Peptide 2 ELISA Kit
Brand: MM
Price: 949 USD
Availability: InStock

measures and quantifies C-Peptide 2 levels in 20 μL serum or plasma

Synonym(s):

C-Peptide 2

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96 WELLS

$949.00

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About This Item

UNSPSC Code:

12161503

eCl@ss:

32161000

NACRES:

NA.32

Key Documents

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Product Name

Rat/Mouse C-Peptide 2 ELISA, This Rat/Mouse C-Peptide 2 ELISA is used to measure & quantify C-Peptide 2 levels in Metabolism & Endocrine & Neuroscience research.

Quality Level

200

species reactivity

mouse, rat

packaging

kit of 1 × 96 wells

parameter

20 μL sample volume (4hr assay)

assay range

accuracy: 86-87%
(Mouse Serum)
accuracy: 88-92%
(Rat Serum)
accuracy: 93-95%
(Rat Plasma)
linearity: 86-108%
standard curve range: 25-1600 pM

technique(s)

ELISA: suitable

input

sample type plasma (K2 EDTA)
sample type serum

application(s)

research use

detection method

colorimetric (450nm/590nm)

shipped in

wet ice

storage temp.

2-8°C

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This Item	EZHCP	EZRMI	EZRMGIP
Millipore EZRMCP2 Rat/Mouse C-Peptide 2 ELISA	Millipore EZHCP Human C-Peptide ELISA	Millipore EZRMI Rat/Mouse Insulin ELISA	Millipore EZRMGIP Rat/Mouse GIP (total) ELISA
species reactivity mouse, rat	species reactivity human	species reactivity mouse, rat	species reactivity mouse, rat
assay range accuracy: 86-87% (Mouse Serum), accuracy: 93-95% (Rat Plasma), standard curve range: 25-1600 pM, accuracy: 88-92% (Rat Serum), linearity: 86-108%	assay range accuracy: 91-111%, linearity: 86-108%, standard curve range: 0.2-20 ng/mL	assay range accuracy: 83-102%, linearity: 79-133%, sensitivity: 0.2 ng/mL, standard curve range: 0.2-10 ng/mL	assay range accuracy: 104.2%, linearity: 100.8%, sensitivity: 8.2 pg/mL, standard curve range: 8.2-2000 pg/mL
input sample type plasma (K2 EDTA) sample type serum	input sample type plasma (K2 EDTA) sample type serum	input sample type serum sample type plasma (K2 EDTA)	input sample type cell culture supernatant sample type plasma (K2 EDTA) sample type serum
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200
detection method colorimetric (450nm/590nm)	detection method colorimetric (450nm)	detection method colorimetric (450nm/590nm)	detection method colorimetric (450nm/590nm)
technique(s) ELISA: suitable	technique(s) ELISA: suitable	technique(s) ELISA: suitable	technique(s) ELISA: suitable

General description

Measurement of C-peptide indicates the pancreatic β-cell function. Compared to endogenous insulin this protein is secreted at a more constant rate and for an extended time. Detection of C-peptide levels helps in diabetes diagnosis and management. The levels of C-peptide determine the type of diabetes and the duration of the disease.

Application

Rat/Mouse C-Peptide 2 ELISA has been used in in vivo experiments to determine the C-peptide levels in mice blood, sera, and plasma.

Features and Benefits

Each kit is sufficient to measure 39 unknown samples in duplicate.

Disclaimer

For research use only. Not for use in diagnostic procedures.

pictograms

GHS05,GHS07

signalword

Warning

hcodes

H290,H317

pcodes

P234 - P261 - P272 - P280 - P302 + P352 - P333 + P313

Hazard Classifications

Met. Corr. 1 - Skin Sens. 1

Storage Class

8A - Combustible corrosive hazardous materials

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A Practical Review of C-Peptide Testing in Diabetes.

Emma Leighton et al.

Diabetes therapy : research, treatment and education of diabetes and related disorders, 8(3), 475-487 (2017-05-10)

C-peptide is a widely used measure of pancreatic beta cell function. It is produced in equimolar amounts to endogenous insulin but is excreted at a more constant rate over a longer time. Methods of estimation include urinary and unstimulated and

Bile acid TUDCA improves insulin clearance by increasing the expression of insulin-degrading enzyme in the liver of obese mice.

Jean Franciesco Vettorazzi et al.

Scientific reports, 7(1), 14876-14876 (2017-11-03)

Disruption of insulin secretion and clearance both contribute to obesity-induced hyperinsulinemia, though reduced insulin clearance seems to be the main factor. The liver is the major site for insulin degradation, a process mainly coordinated by the insulin-degrading enzyme (IDE). The

Partial pancreatic transdifferentiation of primary human hepatocytes in the livers of a humanised mouse model.

Binhai Ren et al.

The journal of gene medicine, 20(5), e3017-e3017 (2018-03-27)

Gene therapy is one treatment that may ultimately cure type 1 diabetes. We have previously shown that the introduction of furin-cleavable human insulin (INS-FUR) to the livers in several animal models of diabetes resulted in the reversal of diabetes and

Administration of Melatonin in Diabetic Retinopathy Is Effective and Improves the Efficacy of Mesenchymal Stem Cell Treatment.

Samraa H Abdel-Kawi et al.

Stem cells international, 2022, 6342594-6342594 (2022-04-23)

Stem cell transplantation is a promising therapeutic technique for the treatment of a variety of diseases; nevertheless, stem cell therapy may not always work as well as it could. The goal of this study was to test the hypothesis that

Energy homeostasis targets chromosomal reconfiguration of the human GH1 locus.

Hana Vakili et al.

The Journal of clinical investigation, 124(11), 5002-5012 (2014-10-09)

Levels of pituitary growth hormone (GH), a metabolic homeostatic factor with strong lipolytic activity, are decreased in obese individuals. GH declines prior to the onset of weight gain in response to excess caloric intake and hyperinsulinemia; however, the mechanism by

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