null

Rat C-Peptide ELISA Kit

SKU:
RTFI00195
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P01322
Sensitivity:
46.875pg/ml
Range:
78.125-5000pg/ml
ELISA Type:
Sandwich
Synonyms:
C-P, C-Peptide, Connecting Peptide
Reactivity:
Rat
Research Area:
Cell Biology
€649
Frequently bought together:

Description

system_update_altDatasheetsystem_update_altMSDS

Rat C-Peptide ELISA Kit

The Rat C-peptide ELISA Kit is specifically designed for the quantitative measurement of C-peptide levels in rat serum, plasma, and tissue extracts. This kit offers exceptional sensitivity and specificity, ensuring accurate and reproducible results for various research applications.C-peptide is a vital peptide produced during proinsulin processing and serves as a marker for insulin secretion. It plays a crucial role in regulating blood sugar levels and assessing beta cell function in diabetes research. The Rat C-peptide ELISA Kit provides researchers with a reliable tool for studying diabetes, pancreatic function, and insulin resistance in rat models.

With its high-quality components and user-friendly protocol, the Rat C-peptide ELISA Kit is a valuable resource for scientists conducting preclinical studies and investigating metabolic disorders in rats. Whether investigating diabetes pathophysiology or evaluating therapeutic interventions, this kit provides a reliable means of quantifying C-peptide levels in rat samples.

Product Name:Rat C-P (C-Peptide) ELISA Kit
Product Code:RTFI00195
Size:96 Assays
Target:Rat C-P
Alias:C-P, C-Peptide, Connecting Peptide
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
Sensitivity:46.875pg/ml
Range:78.125-5000pg/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Rat C-P and the recovery rates were calculated by comparing the measured value to the expected amount of Rat C-P in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)91-10598
EDTA plasma(n=5)87-10497
UFH plasma(n=5)85-10291
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat C-P and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)89-103%94-97%85-102%
EDTA plasma(n=5)88-101%82-97%87-99%
UFH plasma(n=5)84-95%85-98%87-96%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:P13635
UniProt Protein Function:CP: Ceruloplasmin is a blue, copper-binding (6-7 atoms per molecule) glycoprotein. It has ferroxidase activity oxidizing Fe(2+) to Fe(3+) without releasing radical oxygen species. It is involved in iron transport across the cell membrane. Provides Cu(2+) ions for the ascorbate-mediated deaminase degradation of the heparan sulfate chains of GPC1. May also play a role in fetal lung development or pulmonary antioxidant defense. Defects in CP are the cause of aceruloplasminemia (ACERULOP). It is an autosomal recessive disorder of iron metabolism characterized by iron accumulation in the brain as well as visceral organs. Clinical features consist of the triad of retinal degeneration, diabetes mellitus and neurological disturbances. Ceruloplasmin levels are decreased in Wilson disease, in which copper cannot be incorporated into ceruloplasmin in liver because of defects in the copper-transporting ATPase 2. Belongs to the multicopper oxidase family.
UniProt Protein Details:

Protein type:Oxidoreductase; Secreted, signal peptide; EC 1.16.3.1; Secreted; Cofactor and Vitamin Metabolism - porphyrin and chlorophyll

Cellular Component: anchored to plasma membrane; cell; extracellular space; lysosomal membrane

Molecular Function:chaperone binding; copper ion binding; ferroxidase activity

Biological Process: aging; cellular iron ion homeostasis; copper ion transport; liver development; lung development; plasma membrane copper ion transport; response to copper ion; response to nutrient

NCBI Summary:copper-containing ferroxidase that promotes iron incorporation into transferrin; plays a role in iron metabolism and homeostatis [RGD, Feb 2006]
UniProt Code:P13635
NCBI GenInfo Identifier:2506226
NCBI Gene ID:24268
NCBI Accession:P13635.3
UniProt Secondary Accession:P13635,Q64719,
UniProt Related Accession:P13635
Molecular Weight:120,841 Da
NCBI Full Name:Ceruloplasmin
NCBI Synonym Full Names:ceruloplasmin (ferroxidase)
NCBI Official Symbol:Cp  
NCBI Official Synonym Symbols:CERP  
NCBI Protein Information:ceruloplasmin
UniProt Protein Name:Ceruloplasmin
UniProt Synonym Protein Names:Ferroxidase
Protein Family:Ceruloplasmin
UniProt Gene Name:Cp  
UniProt Entry Name:CERU_RAT
StepProcedure
1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!
2.Aliquot 0.1ml standard solutions into the standard wells.
3. Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well.
4. Add 0.1 ml of properly diluted sample ( Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells.
5.Seal the plate with a cover and incubate at 37°C for 90 min.
6. Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2.
7. Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall.
8.Seal the plate with a cover and incubate at 37°C for 60 min.
9. Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash.
10. Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min.
11. Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min.
12. Add 90 µL of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color.
13. Add 50 µL of Stop solution into each well and mix thoroughly. The color changes into yellow immediately.
14. Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution.

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample Type Protocol
Serum:

If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

If serum separator tubes are not being used, allow samples to clotovernight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Removeserum and assay promptly or aliquot and store the samples at-80°C. Avoid multiple freeze-thaw cycles.

Plasma: Collect plasma using EDTA or heparin as an anti-coagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.Note: Over haemolysed samples are not suitable for use with this kit.
Urine & Cerebrospinal Fluid: Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.
Cell Culture Supernatant: Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.
Cell Lysates: Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20°C.
Tissue Homogenates: The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenizein 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or-80°C.
Tissue Lysates: Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Breast Milk: Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

Related Products