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Mouse Renin ELISA Kit (MOFI01082)

SKU:
MOFI01082
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P06281
Sensitivity:
56.25pg/ml
Range:
93.75-6000pg/ml
ELISA Type:
Sandwich
Synonyms:
REN, Renin, Angiotensinogenase, angiotensin-forming enzyme, HNFJ2, renin precursor, renal
Reactivity:
Mouse
Research Area:
Cell Cycle
€649
Frequently bought together:

Description

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Mouse Renin ELISA Kit

The Mouse Renin ELISA Kit is specifically designed for the precise measurement of renin levels in mouse serum, plasma, and tissue culture supernatants. This kit is characterized by its exceptional sensitivity and specificity, ensuring accurate and consistent results, thus making it the perfect tool for a variety of research purposes.Renin is a key enzyme in the renin-angiotensin system, playing a vital role in blood pressure regulation and electrolyte balance.

Dysregulation of renin levels has been linked to hypertension, kidney disease, and other cardiovascular conditions, making it a critical biomarker for understanding these diseases and developing potential treatment strategies.With the Mouse Renin ELISA Kit, researchers can confidently study the role of renin in various biological processes and diseases, paving the way for advancements in the field of cardiovascular research.

Product Name:Mouse Renin ELISA Kit
Product Code:MOFI01082
Size:96 Assays
Alias:REN, Renin, Angiotensinogenase, angiotensin-forming enzyme, HNFJ2, renin precursor, renal
Detection Method:Sandwich ELISA
Application:This immunoassay kit allows for the in vitro quantitative determination of Mouse REN concentrations in serum plasma and other biological fluids.
Sensitivity:56.25pg/ml
Range:93.75-6000pg/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of Mouse REN and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse REN in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)93-10297
EDTA plasma(n=5)87-10492
UFH plasma(n=5)88-10398
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse REN and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)89-101%91-104%86-101%
EDTA plasma(n=5)86-97%87-94%85-99%
UFH plasma(n=5)84-100%80-97%81-99%
Intra Assay:CV <8%
Inter Assay:CV <10%
ComponentQuantityStorage
ELISA Microplate (Dismountable)8×12 strips4°C for 6 months
Lyophilized Standard24°C/-20°C
Sample/Standard Dilution Buffer20ml4°C
Biotin-labeled Antibody(Concentrated)120ul4°C (Protect from light)
Antibody Dilution Buffer10ml4°C
HRP-Streptavidin Conjugate(SABC)120ul4°C (Protect from light)
SABC Dilution Buffer10ml4°C
TMB Substrate10ml4°C (Protect from light)
Stop Solution10ml4°C
Wash Buffer(25X)30ml4°C
Plate Sealer5-

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
UniprotP06281
UniProt Protein Function:REN: Renin is a highly specific endopeptidase, whose only known function is to generate angiotensin I from angiotensinogen in the plasma, initiating a cascade of reactions that produce an elevation of blood pressure and increased sodium retention by the kidney. Interacts with ATP6AP2. Interaction with ATP6AP2 results in a 5-fold increased efficiency in angiotensinogen processing. Belongs to the peptidase A1 family. 2 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Secreted; EC 3.4.23.15; Protease; Secreted, signal peptide

Cellular Component: extracellular space; membrane; cytoplasm; extracellular region; intracellular

Molecular Function:peptidase activity; insulin-like growth factor receptor binding; hydrolase activity; endopeptidase activity; aspartic-type endopeptidase activity; receptor binding

Biological Process: response to drug; response to cAMP; establishment of blood-nerve barrier; hormone-mediated signaling; cell maturation; renin-angiotensin regulation of aldosterone production; drinking behavior; angiotensin maturation; proteolysis; response to organic substance; regulation of MAPKKK cascade; regulation of blood pressure; renin-angiotensin regulation of blood volume; kidney development

UniProt Code:P06281
NCBI GenInfo Identifier:132327
NCBI Gene ID:19701
NCBI Accession:P06281.1
UniProt Secondary Accession:P06281,P97911, Q543E5, Q62153, Q62154,
UniProt Related Accession:P06281
Molecular Weight:44,343 Da
NCBI Full Name:Renin-1
NCBI Synonym Full Names:renin 1 structural
NCBI Official Symbol:Ren1  
NCBI Official Synonym Symbols:Ren; Rnr; Rn-1; Ren-1; Ren-A; Ren1c; Ren1d; D19352  
NCBI Protein Information:renin-1; renin b; kidney renin; aspartyl-protease; angiotensinogenase
UniProt Protein Name:Renin-1
UniProt Synonym Protein Names:Angiotensinogenase; Kidney renin
Protein Family:Renin
UniProt Gene Name:Ren1  
UniProt Entry Name:RENI1_MOUSE

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

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 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.

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