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Human Atrial natriuretic peptide-converting enzyme (CORIN) ELISA Kit (HUEB0297)

SKU:
HUEB0297
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q9Y5Q5
Range:
78-5000 pg/mL
ELISA Type:
Sandwich
Reactivity:
Human
€599
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Description

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Human Atrial natriuretic peptide-converting enzyme (CORIN) ELISA Kit

The Human Atrial Natriuretic Peptide Converting Enzyme (Corin) ELISA Kit is a highly sensitive and specific assay designed for the accurate detection of corin levels in human serum, plasma, and cell culture supernatants. This kit provides reliable and reproducible results, making it ideal for a wide range of research applications.Corin is a critical enzyme involved in the regulation of atrial natriuretic peptide, a hormone that plays a crucial role in blood pressure regulation and fluid balance.

Dysregulation of corin has been linked to conditions such as hypertension, heart failure, and kidney disease, making it an important biomarker for studying these conditions and developing potential interventions.Overall, the Human Atrial Natriuretic Peptide Converting Enzyme (Corin) ELISA Kit is a valuable tool for researchers looking to study the role of corin in various physiological and pathological processes, providing accurate and precise measurements for insightful research outcomes.

Product Name:Human Atrial natriuretic peptide-converting enzyme (CORIN) ELISA Kit
SKU:HUEB0297
Size:96T
Target:Human Atrial natriuretic peptide-converting enzyme (CORIN)
Synonyms:Corin, Heart-specific serine proteinase ATC2, Pro-ANP-converting enzyme, Transmembrane protease serine 10, CRN, TMPRSS10
Assay Type:Sandwich
Detection Method:ELISA
Reactivity:Human
Detection Range:78-5000pg/mL
Sensitivity:34pg/mL
Intra CV:6.1%
Inter CV:11.3%
Linearity:
Sample1:21:41:81:16
Serum(N=5)104-116%115-125%92-104%101-111%
EDTA Plasma(N=5)93-103%106-116%82-90%99-109%
Heparin Plasma(N=5)82-95%106-114%94-103%95-105%
Recovery:
Sample TypeAverage(%)Recovery Range(%)
Serum111105-117
Plasma113107-119
Function:Isoform 2: has weaker endopeptidase activity compared to isoform 1.
Uniprot:Q9Y5Q5
Sample Type:Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Specificity:Natural and recombinant human Atrial natriuretic peptide-converting enzyme
Subcellular Location:Atrial natriuretic peptide-converting enzyme, 100 kDa soluble fragment Secreted Soluble form produced following autocatalytic cleavage.
Storage:Please see kit components below for exact storage details
Note:For research use only
UniProt Protein Function:CORIN: Serine-type endopeptidase involved in atrial natriuretic peptide hormone (NPPA) processing. Converts through proteolytic cleavage the non-functional propeptide NPPA into the active hormone, thereby regulating blood pressure in heart and promoting natriuresis, diuresis and vasodilation. Proteolytic cleavage of pro-NPPA also plays a role in female pregnancy by promoting trophoblast invasion and spiral artery remodeling in uterus. Also acts as a regulator of sodium reabsorption in kidney. May also process pro-NPPB the B-type natriuretic peptide. Defects in CORIN are the cause of pre-eclampsia/eclampsia 5 (PEE5); also known as gestational proteinuric hypertension. Preeclampsia is a pregnancy-associated disease with maternal symptoms but placental origin. Unlike most other human disorders, it impacts 2 individuals, the mother and her child, both of whom can be severely affected. Belongs to the peptidase S1 family. 2 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:EC 3.4.21.-; Membrane protein, integral; Cell surface; Protease

Chromosomal Location of Human Ortholog: 4p12

Cellular Component: plasma membrane

Molecular Function:serine-type endopeptidase activity

Biological Process: female pregnancy; peptide hormone processing; regulation of blood pressure; regulation of systemic arterial blood pressure by atrial natriuretic peptide

Disease: Preeclampsia/eclampsia 5

NCBI Summary:This gene encodes a member of the type II transmembrane serine protease class of the trypsin superfamily. Members of this family are composed of multiple structurally distinct domains. The encoded protein converts pro-atrial natriuretic peptide to biologically active atrial natriuretic peptide, a cardiac hormone that regulates blood volume and pressure. This protein may also function as a pro-brain-type natriuretic peptide convertase. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2013]
UniProt Code:Q9Y5Q5
NCBI GenInfo Identifier:317373348
NCBI Gene ID:10699
NCBI Accession:Q9Y5Q5.2
UniProt Secondary Accession:Q9Y5Q5,Q2TBD2, Q4W5E5, Q4W5G6, Q9UHY2, B0ZBE3,
UniProt Related Accession:Q9Y5Q5
Molecular Weight:113,297 Da
NCBI Full Name:Atrial natriuretic peptide-converting enzyme
NCBI Synonym Full Names:corin, serine peptidase
NCBI Official Symbol:CORIN
NCBI Official Synonym Symbols:CRN; ATC2; Lrp4; PEE5; TMPRSS10
NCBI Protein Information:atrial natriuretic peptide-converting enzyme
UniProt Protein Name:Atrial natriuretic peptide-converting enzyme
UniProt Synonym Protein Names:Corin; Heart-specific serine proteinase ATC2; Pro-ANP-converting enzyme; Transmembrane protease serine 10
Protein Family:Atrial natriuretic peptide-converting enzyme
UniProt Gene Name:CORIN
UniProt Entry Name:CORIN_HUMAN
Component Quantity (96 Assays) Storage
ELISA Microplate (Dismountable) 8×12 strips -20°C
Lyophilized Standard 2 -20°C
Sample Diluent 20ml -20°C
Assay Diluent A 10mL -20°C
Assay Diluent B 10mL -20°C
Detection Reagent A 120µL -20°C
Detection Reagent B 120µL -20°C
Wash Buffer 30mL 4°C
Substrate 10mL 4°C
Stop Solution 10mL 4°C
Plate Sealer 5 -

Other materials and equipment required:

  • Microplate reader with 450 nm wavelength filter
  • Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
  • Incubator
  • Deionized or distilled water
  • Absorbent paper
  • Buffer resevoir

*Note: The below protocol is a sample protocol. Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.

Allow all reagents to reach room temperature (Please do not dissolve the reagents at 37°C directly). All the reagents should be mixed thoroughly by gently swirling before pipetting. Avoid foaming. Keep appropriate numbers of strips for 1 experiment and remove extra strips from microtiter plate. Removed strips should be resealed and stored at -20°C until the kits expiry date. Prepare all reagents, working standards and samples as directed in the previous sections. Please predict the concentration before assaying. If values for these are not within the range of the standard curve, users must determine the optimal sample dilutions for their experiments. We recommend running all samples in duplicate.

Step
1. Add Sample: Add 100µL of Standard, Blank, or Sample per well. The blank well is added with Sample diluent. Solutions are added to the bottom of micro ELISA plate well, avoid inside wall touching and foaming as possible. Mix it gently. Cover the plate with sealer we provided. Incubate for 120 minutes at 37°C.
2. Remove the liquid from each well, don't wash. Add 100µL of Detection Reagent A working solution to each well. Cover with the Plate sealer. Gently tap the plate to ensure thorough mixing. Incubate for 1 hour at 37°C. Note: if Detection Reagent A appears cloudy warm to room temperature until solution is uniform.
3. Aspirate each well and wash, repeating the process three times. Wash by filling each well with Wash Buffer (approximately 400µL) (a squirt bottle, multi-channel pipette,manifold dispenser or automated washer are needed). Complete removal of liquid at each step is essential. After the last wash, completely remove remaining Wash Buffer by aspirating or decanting. Invert the plate and pat it against thick clean absorbent paper.
4. Add 100µL of Detection Reagent B working solution to each well. Cover with the Plate sealer. Incubate for 60 minutes at 37°C.
5. Repeat the wash process for five times as conducted in step 3.
6. Add 90µL of Substrate Solution to each well. Cover with a new Plate sealer and incubate for 10-20 minutes at 37°C. Protect the plate from light. The reaction time can be shortened or extended according to the actual color change, but this should not exceed more than 30 minutes. When apparent gradient appears in standard wells, user should terminatethe reaction.
7. Add 50µL of Stop Solution to each well. If color change does not appear uniform, gently tap the plate to ensure thorough mixing.
8. Determine the optical density (OD value) of each well at once, using a micro-plate reader set to 450 nm. User should open the micro-plate reader in advance, preheat the instrument, and set the testing parameters.
9. After experiment, store all reagents according to the specified storage temperature respectively until their expiry.

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 clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum 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 anticoagulant. 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 & homogenize in 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.
ELISAAntibodies
Human CRN (Corin) CLIA Kit (HUES00041)Anti-CORIN Antibody (CAB10404)
Human CRN (Corin) ELISA Kit (HUES01329)YME1L1 Antibody (PACO45638)
CORIN Antibody (PACO45639)

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