Mouse NCOR2 ELISA Kit

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SKU:
MOFI00223
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q9WU42
Sensitivity:
37.5pg/ml
Range:
62.5-4000pg/ml
ELISA Type:
Sandwich ELISA, Double Antibody
Synonyms:
Ncor2, CTG26, SMRT, SMRTE, TNRC14, TRAC-1, CTG repeat protein 26, CTG26nuclear receptor co-repressor 2, FLJ25011, N-CoR2, nuclear receptor corepressor 2, retinoic-acid-receptor-associated corepressor, silencing mediator for retinoid and thyroid hormo
Reactivity:
Mouse
€0.00
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Description

system_update_alt데이터시트system_update_alt안전 데이터시트
Product Name:Mouse NCOR2 ELISA Kit
Product Code:MOFI00223
Size:96 Assays
Alias:Ncor2, CTG26, SMRT, SMRTE, TNRC14, TRAC-1, CTG repeat protein 26, CTG26nuclear receptor co-repressor 2, FLJ25011, N-CoR2, nuclear receptor corepressor 2, retinoic-acid-receptor-associated corepressor, silencing mediator for retinoid and thyroid hormone receptors, SMAP270, SMRTE, SMRTE-tau, SMRTT3 receptor-associating factor, TNRC14, TRAC, TRAC1
Detection Method:Sandwich ELISA
Application:This immunoassay kit allows for the in vitro quantitative determination of Mouse Ncor2 concentrations in serum plasma and other biological fluids.
Sensitivity:37.5pg/ml
Range:62.5-4000pg/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Mouse Ncor2 and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse Ncor2 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)85-10495
EDTA plasma(n=5)93-10598
UFH plasma(n=5)87-10192
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse Ncor2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)86-96%93-102%87-104%
EDTA plasma(n=5)85-100%90-96%83-100%
UFH plasma(n=5)83-96%82-100%82-100%
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
UniprotQ9WU42
UniProt Protein Function:SMRT: Transcriptional corepressor of NR4A2/NURR1 and acts through histone deacetylases (HDACs) to keep promoters of NR4A2/NURR1 target genes in a repressed deacetylated state. Mediates the transcriptional repression activity of some nuclear receptors by promoting chromatin condensation, thus preventing access of the basal transcription. Isoform 1 and isoform 5 have different affinities for different nuclear receptors. Interacts with BCL6, HDAC7 and C1D. Interacts with NR4A2; this interaction increases in the absence of PITX3. Forms a large corepressor complex that contains SIN3A/B and histone deacetylases HDAC1 and HDAC2. This complex associates with the thyroid (TR) and the retinoid acid receptors (RAR) in the absence of ligand, and may stabilize their interaction with TFIIB. Interacts directly with RARA in the absence of ligand; the interaction represses RARA activity. Interacts (isoform SRMT) with HDAC10. Interacts with MINT. Component of the N-Cor repressor complex, at least composed of NCOR1, NCOR2, HDAC3, TBL1X, TBL1R, CORO2A and GPS2. Interacts with CBFA2T3 and ATXN1L. Interacts with RARB; the interaction is weak and does not repress RARB transactivational activity. Regulated during cell cycle progression. Ubiquitous. High levels of expression are detected in lung, spleen and brain. Belongs to the N-CoR nuclear receptor corepressors family. 5 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Nuclear receptor co-regulator; Transcription, coactivator/corepressor

Cellular Component: chromatin; histone deacetylase complex; membrane; nuclear body; nuclear matrix; nucleoplasm; nucleus; transcriptional repressor complex

Molecular Function:chromatin binding; DNA binding; glucocorticoid receptor binding; histone deacetylase binding; ligand-dependent nuclear receptor binding; Notch binding; protein binding; protein complex binding; protein N-terminus binding; retinoic acid receptor binding; retinoid X receptor binding; sequence-specific DNA binding; transcription corepressor activity; transcription factor binding

Biological Process: cell proliferation in forebrain; forebrain development; glucose homeostasis; heart morphogenesis; in utero embryonic development; negative regulation of fat cell differentiation; negative regulation of transcription from RNA polymerase II promoter; negative regulation of transcription, DNA-dependent; regulation of transcription, DNA-dependent; telencephalon development; transcription, DNA-dependent; white fat cell differentiation

UniProt Code:Q9WU42
NCBI GenInfo Identifier:359806942
NCBI Gene ID:20602
NCBI Accession:NP_001240833.1
UniProt Secondary Accession:Q9WU42,Q9WU43, Q9WUC1, E9Q9V0,
UniProt Related Accession:Q9WU42
Molecular Weight:245,029 Da
NCBI Full Name:nuclear receptor corepressor 2 isoform 2
NCBI Synonym Full Names:nuclear receptor co-repressor 2
NCBI Official Symbol:Ncor2  
NCBI Official Synonym Symbols:SMRT; N-CoR; SMRTe  
NCBI Protein Information:nuclear receptor corepressor 2
UniProt Protein Name:Nuclear receptor corepressor 2
UniProt Synonym Protein Names:Silencing mediator of retinoic acid and thyroid hormone receptor; SMRT; SMRTe; T3 receptor-associating factor; TRAC; Thyroid-, retinoic-acid-receptor-associated corepressor
Protein Family:Nuclear receptor corepressor
UniProt Gene Name:Ncor2  
UniProt Entry Name:NCOR2_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 TypeProtocol
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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