Mouse IDE / Insulin-degrading enzyme ELISA Kit
- SKU:
- MOFI00503
- Product Type:
- ELISA Kit
- Size:
- 96 Assays
- Uniprot:
- Q9JHR7
- Sensitivity:
- 0.188ng/ml
- Range:
- 0.313-20ng/ml
- ELISA Type:
- Sandwich
- Synonyms:
- Ide, IDE, INSDEGM, Insulinase, Abeta-degrading protease, EC 3.4.24, EC 3.4.24.56, FLJ35968, Insulin protease, insulinase, Insulinase, insulin-degrading enzyme, INSULYSIN, Insulysin
- Reactivity:
- Mouse
Description
Mouse IDE/Insulin-degrading enzyme ELISA Kit
The Mouse IDE (Insulin Degrading Enzyme) ELISA Kit is a highly accurate and reliable tool for the detection of IDE levels in mouse serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring precise and consistent results for a variety of research applications.IDE is an important enzyme involved in the regulation of insulin levels and degradation, playing a critical role in maintaining glucose homeostasis. Dysregulation of IDE has been linked to conditions such as diabetes and Alzheimer's disease, making it a valuable biomarker for studying these diseases and identifying potential therapeutic targets.
Overall, the Mouse IDE ELISA Kit is a valuable tool for researchers looking to explore the role of IDE in disease pathogenesis and potential therapeutic interventions. Its high-quality performance and ease of use make it a valuable addition to any laboratory conducting studies in the fields of diabetes, neurodegenerative disorders, and metabolic diseases.
| Product Name: | Mouse IDE / Insulin-degrading enzyme ELISA Kit |
| Product Code: | MOFI00503 |
| Size: | 96 Assays |
| Alias: | Ide, IDE, INSDEGM, Insulinase, Abeta-degrading protease, EC 3.4.24, EC 3.4.24.56, FLJ35968, Insulin protease, insulinase, Insulinase, insulin-degrading enzyme, INSULYSIN, Insulysin |
| Detection Method: | Sandwich ELISA |
| Application: | This immunoassay kit allows for the in vitro quantitative determination of Mouse Ide concentrations in serum plasma and other biological fluids. |
| Sensitivity: | 0.188ng/ml |
| Range: | 0.313-20ng/ml |
| Storage: | 4°C for 6 months |
| Note: | For Research Use Only |
| Recovery: | Matrices listed below were spiked with certain level of Mouse Ide and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse Ide in samples. | ||||||||||||||||
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| Linearity: | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse Ide and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected. | ||||||||||||||||
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| Intra Assay: | CV <8% | ||||||||||||||||
| Inter Assay: | CV <10% |
| Component | Quantity | Storage |
| ELISA Microplate (Dismountable) | 8-12 strips | 4°C for 6 months |
| Lyophilized Standard | 2 | 4°C/-20°C |
| Sample/Standard Dilution Buffer | 20ml | 4°C |
| Biotin-labeled Antibody(Concentrated) | 120ul | 4°C (Protect from light) |
| Antibody Dilution Buffer | 10ml | 4°C |
| HRP-Streptavidin Conjugate(SABC) | 120ul | 4°C (Protect from light) |
| SABC Dilution Buffer | 10ml | 4°C |
| TMB Substrate | 10ml | 4°C (Protect from light) |
| Stop Solution | 10ml | 4°C |
| Wash Buffer(25X) | 30ml | 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
| Uniprot | Q9JHR7 |
| UniProt Protein Function: | IDE: Plays a role in the cellular breakdown of insulin, IAPP, glucagon, bradykinin, kallidin and other peptides, and thereby plays a role in intercellular peptide signaling. Degrades amyloid formed by APP and IAPP. May play a role in the degradation and clearance of naturally secreted amyloid beta-protein by neurons and microglia. Belongs to the peptidase M16 family. 2 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:EC 3.4.24.56; Cell surface; Nuclear receptor co-regulator; Protease Cellular Component: cell surface; cytoplasm; cytosol; extracellular region; extracellular space; membrane; mitochondrion; nucleoplasm; nucleus; peroxisomal matrix; peroxisome; plasma membrane Molecular Function:ATP binding; ATPase activity; beta-amyloid binding; beta-endorphin binding; catalytic activity; glycoprotein binding; hydrolase activity; insulin binding; metal ion binding; metalloendopeptidase activity; metallopeptidase activity; nucleotide binding; peptidase activity; peptide binding; peptide hormone binding; protein homodimerization activity; receptor binding; ubiquitin binding; zinc ion binding Biological Process: beta-amyloid metabolic process; cellular protein catabolic process; determination of adult life span; hormone catabolic process; metabolic process; negative regulation of proteolysis; peptide catabolic process; positive regulation of protein oligomerization; protein heterooligomerization; protein homooligomerization; protein homotetramerization; protein processing; proteolysis; proteolysis involved in cellular protein catabolic process |
| UniProt Code: | Q9JHR7 |
| NCBI GenInfo Identifier: | 14548072 |
| NCBI Gene ID: | 15925 |
| NCBI Accession: | Q9JHR7.1 |
| UniProt Related Accession: | Q9JHR7 |
| Molecular Weight: | 117,772 Da |
| NCBI Full Name: | Insulin-degrading enzyme |
| NCBI Synonym Full Names: | insulin degrading enzyme |
| NCBI Official Symbol: | Ide  |
| NCBI Official Synonym Symbols: | AA675336; AI507533; 1300012G03Rik; 4833415K22Rik  |
| NCBI Protein Information: | insulin-degrading enzyme |
| UniProt Protein Name: | Insulin-degrading enzyme |
| UniProt Synonym Protein Names: | Insulin protease; Insulinase; Insulysin |
| Protein Family: | IgM protease |
| UniProt Gene Name: | Ide  |
| UniProt Entry Name: | IDE_MOUSE |
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
| Step | Procedure |
| 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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