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Mouse Indoleamine 2,3-dioxygenase 1 (Ido1) ELISA Kit (MOEB1510)

SKU:
MOEB1510
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P28776
Range:
0.78-50 ng/mL
ELISA Type:
Sandwich
Synonyms:
Ido1, IDO1, INDO, IDOIDO-1, INDOindole 2, 3-dioxygenase, indoleamine 2, 3-dioxygenase 1, indoleamine-pyrrole 2, 3 dioxygenase, Indoleamine-pyrrole 2, 3-dioxygenase
Reactivity:
Mouse
€649
Frequently bought together:

Description

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Mouse Indoleamine 2,3-dioxygenase 1 (Ido1) ELISA Kit

The Mouse Indoleamine 2,3-dioxygenase 1 (IDO1) ELISA Kit is a highly reliable and accurate tool for the detection of IDO1 levels in mouse serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring consistent and precise results for a variety of research applications.IDO1 is an enzyme that plays a critical role in regulating the immune response by catalyzing the breakdown of tryptophan. Dysregulation of IDO1 has been implicated in various diseases, including cancer, autoimmune disorders, and infectious diseases.

Therefore, measuring IDO1 levels can provide valuable insights into disease progression and potential therapeutic targets.With its superior performance and ease of use, the Mouse IDO1 ELISA Kit is an indispensable tool for researchers studying the role of IDO1 in immune regulation and disease pathogenesis. Get accurate and reliable results with this cutting-edge kit from AssayGenie.

Product Name:Mouse Indoleamine 2,3-dioxygenase 1 (Ido1) ELISA Kit
SKU:MOEB1510
Size:96T
Target:Mouse Indoleamine 2,3-dioxygenase 1 (Ido1)
Synonyms:Indoleamine-pyrrole 2, 3-dioxygenase, IDO-1, Ido, Indo
Assay Type:Sandwich
Detection Method:ELISA
Reactivity:Mouse
Detection Range:0.78-50ng/mL
Sensitivity:0.4ng/mL
Intra CV:5.3%
Inter CV:7.7%
Linearity:
Sample1:21:41:81:16
Serum(N=5)89-99%80-89%84-92%100-110%
EDTA Plasma(N=5)103-111%80-90%83-92%103-113%
Heparin Plasma(N=5)88-97%107-116%88-98%92-103%
Recovery:
Sample TypeAverage(%)Recovery Range(%)
Serum9185-97
Plasma9387-99
Function:Catalyzes the first and rate limiting step of the catabolism of the essential amino acid tryptophan along the kynurenine pathway. Involved in the peripheral immune tolerance, contributing to maintain homeostasis by preventing autoimmunity or immunopathology that would result from uncontrolled and overreacting immune responses. Tryptophan shortage inhibits T lymphocytes division and accumulation of tryptophan catabolites induces T-cell apoptosis and differentiation of regulatory T-cells. Acts as a suppressor of anti-tumor immunity (PubMed:25691885). Limits the growth of intracellular pathogens by depriving tryptophan. Protects the fetus from maternal immune rejection (Ref. 3).
Uniprot:P28776
Sample Type:Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Specificity:Natural and recombinant mouse Indoleamine 2,3-dioxygenase 1
Sub Unit:Monomer.
Research Area:Cell Biology
Subcellular Location:Cytoplasm Cytosol
Storage:Please see kit components below for exact storage details
Note:For research use only
UniProt Protein Function:INDO: Catalyzes the cleavage of the pyrrol ring of tryptophan and incorporates both atoms of a molecule of oxygen. Belongs to the indoleamine 2,3-dioxygenase family.
UniProt Protein Details:

Protein type:Amino Acid Metabolism - tryptophan; Oxidoreductase; EC 1.13.11.52; Cell cycle regulation

Cellular Component: cytoplasm; cytosol; smooth muscle contractile fiber; stereocilium bundle

Molecular Function:amino acid binding; dioxygenase activity; heme binding; indoleamine 2,3-dioxygenase activity; metal ion binding; oxidoreductase activity; oxygen binding; protein binding; tryptophan 2,3-dioxygenase activity

Biological Process: cytokine production during acute inflammatory response; defense response; immune system process; inflammatory response; multicellular organismal response to stress; negative regulation of activated T cell proliferation; negative regulation of interleukin-10 production; negative regulation of T cell proliferation; positive regulation of apoptosis; positive regulation of chronic inflammatory response; positive regulation of interleukin-12 production; positive regulation of T cell tolerance induction; positive regulation of T-helper 2 type immune response; response to lipopolysaccharide; tryptophan catabolic process; tryptophan catabolic process to kynurenine

UniProt Code:P28776
NCBI GenInfo Identifier:123949
NCBI Gene ID:15930
NCBI Accession:P28776.1
UniProt Related Accession:P28776
Molecular Weight:45,641 Da
NCBI Full Name:Indoleamine 2,3-dioxygenase 1
NCBI Synonym Full Names:indoleamine 2,3-dioxygenase 1
NCBI Official Symbol:Ido1
NCBI Official Synonym Symbols:Ido; Indo
NCBI Protein Information:indoleamine 2,3-dioxygenase 1
UniProt Protein Name:Indoleamine 2,3-dioxygenase 1
UniProt Synonym Protein Names:Indoleamine-pyrrole 2,3-dioxygenase
Protein Family:Indoleamine 2,3-dioxygenase
UniProt Gene Name:Ido1
UniProt Entry Name:I23O1_MOUSE
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.

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