SF1 (Phospho-Ser82) Colorimetric Cell-Based ELISA Kit
- SKU:
- CBCAB01318
- Product Type:
- ELISA Kit
- ELISA Type:
- Cell Based Phospho Specific
- Research Area:
- Epigenetics and Nuclear Signaling
- Reactivity:
- Human
- Mouse
- Detection Method:
- Colorimetric
Description
SF1 (Phospho-Ser82)Colorimetric Cell-Based ELISA Kit
The SF1 (Phospho-Ser82) Colorimetric Cell-Based ELISA Kit is a cutting-edge assay designed for the precise measurement of SF1 phosphorylation at serine 82 in cell lysates. This kit offers high sensitivity and specificity, ensuring accurate and reproducible results for your research needs.SF1, also known as splicing factor 1, plays a crucial role in alternative splicing, gene regulation, and RNA processing. Phosphorylation of SF1 at serine 82 has been linked to various cellular processes and diseases, making it a valuable target for studying signal transduction pathways and potential therapeutic interventions.
With the SF1 (Phospho-Ser82) Colorimetric Cell-Based ELISA Kit, researchers can explore the role of SF1 phosphorylation in cellular functions and disease pathways, paving the way for new insights and discoveries in the field of molecular biology and drug development.
| Product Name: | SF1 (Phospho-Ser82) Colorimetric Cell-Based ELISA |
| Product Code: | CBCAB01318 |
| ELISA Type: | Cell-Based |
| Target: | SF1 (Phospho-Ser82) |
| Reactivity: | Human, Mouse |
| Dynamic Range: | > 5000 Cells |
| Detection Method: | Colorimetric 450 nm |
| Format: | 2 x 96-Well Microplates |
The SF1 (Phospho-Ser82) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect SF1 protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated SF1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on SF1 phosphorylation.
Qualitative determination of SF1 (Phospho-Ser82) concentration is achieved by an indirect ELISA format. In essence, SF1 (Phospho-Ser82) is captured by SF1 (Phospho-Ser82)-specific primary (1ø) antibodies while the HRP-conjugated secondary (2ø) antibodies bind the Fc region of the 1ø antibody. Through this binding, the HRP enzyme conjugated to the 2ø antibody can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of the Cell-Based ELISA, multiple normalization methods are needed:
| 1. | A monoclonal antibody specific for human GAPDH is included to serve as an internal positive control in normalizing the target absorbance values. |
| 2. | Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method may be used to determine cell density. After staining, the results can be analysed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted. |
| Database Information: | Gene ID: 7536, UniProt ID: Q15637, OMIM: 601516, Unigene: Hs.502829/Hs.708209 |
| Gene Symbol: | SF1 |
| Sub Type: | Phospho |
| UniProt Protein Function: | SF1: a splicing factor necessary for the ATP-dependent first step of spliceosome assembly. Binds to the intron branch point sequence (BPS) 5'-UACUAAC-3' of the pre-mRNA. May act as transcription repressor. Phosphorylation of SF1 by cGMP-dependent protein kinase regulates spliceosome assembly. Binds U2AF2. Interacts with U1 snRNA. Binds EWSR1, FUS and TAF15. Six alternatively spliced isoforms have been described. |
| UniProt Protein Details: | Protein type:Transcription, coactivator/corepressor; Spliceosome; RNA splicing; RNA-binding Chromosomal Location of Human Ortholog: 11q13 Cellular Component: nucleoplasm; spliceosome; ribosome; nucleus Molecular Function:zinc ion binding; RNA binding; transcription corepressor activity Biological Process: nuclear mRNA 3'-splice site recognition; nuclear mRNA splicing, via spliceosome; Leydig cell differentiation; regulation of transcription, DNA-dependent; transcription, DNA-dependent; negative regulation of smooth muscle cell proliferation; male sex determination; spliceosome assembly; regulation of steroid biosynthetic process |
| NCBI Summary: | This gene encodes a nuclear pre-mRNA splicing factor. The encoded protein specifically recognizes the intron branch point sequence and is required for the early stages of spliceosome assembly. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
| UniProt Code: | Q15637 |
| NCBI GenInfo Identifier: | 38258418 |
| NCBI Gene ID: | 7536 |
| NCBI Accession: | Q15637.4 |
| UniProt Secondary Accession: | Q15637,Q14818, Q14819, Q15913, Q8IY00, Q92744, Q92745 Q969H7, Q9BW01, Q9UEI0, B7Z1Q1, C9JJE2, |
| UniProt Related Accession: | Q15637 |
| Molecular Weight: | 65,371 Da |
| NCBI Full Name: | Splicing factor 1 |
| NCBI Synonym Full Names: | splicing factor 1 |
| NCBI Official Symbol: | SF1 |
| NCBI Official Synonym Symbols: | BBP; MBBP; ZFM1; ZNF162; D11S636; ZCCHC25 |
| NCBI Protein Information: | splicing factor 1; zinc finger protein 162; transcription factor ZFM1; zinc finger gene in MEN1 locus; mammalian branch point-binding protein |
| UniProt Protein Name: | Splicing factor 1 |
| UniProt Synonym Protein Names: | Mammalian branch point-binding protein; BBP; mBBP; Transcription factor ZFM1; Zinc finger gene in MEN1 locus; Zinc finger protein 162 |
| Protein Family: | Splicing factor |
| UniProt Gene Name: | SF1 |
| UniProt Entry Name: | SF01_HUMAN |
| Component | Quantity |
| 96-Well Cell Culture Clear-Bottom Microplate | 2 plates |
| 10X TBS | 24 mL |
| Quenching Buffer | 24 mL |
| Blocking Buffer | 50 mL |
| 15X Wash Buffer | 50 mL |
| Primary Antibody Diluent | 12 mL |
| 100x Anti-Phospho Target Antibody | 60 µL |
| 100x Anti-Target Antibody | 60 µL |
| Anti-GAPDH Antibody | 60 µL |
| HRP-Conjugated Anti-Rabbit IgG Antibody | 12 mL |
| HRP-Conjugated Anti-Mouse IgG Antibody | 12 mL |
| SDS Solution | 12 mL |
| Stop Solution | 24 mL |
| Ready-to-Use Substrate | 12 mL |
| Crystal Violet Solution | 12 mL |
| Adhesive Plate Seals | 2 seals |
The following materials and/or equipment are NOT provided in this kit but are necessary to successfully conduct the experiment:
- Microplate reader able to measure absorbance at 450 nm and/or 595 nm for Crystal Violet Cell Staining (Optional)
- Micropipettes with capability of measuring volumes ranging from 1 µL to 1 ml
- 37% formaldehyde (Sigma Cat# F-8775) or formaldehyde from other sources
- Squirt bottle, manifold dispenser, multichannel pipette reservoir or automated microplate washer
- Graph paper or computer software capable of generating or displaying logarithmic functions
- Absorbent papers or vacuum aspirator
- Test tubes or microfuge tubes capable of storing ≥1 ml
- Poly-L-Lysine (Sigma Cat# P4832 for suspension cells)
- Orbital shaker (optional)
- Deionized or sterile water
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
| Step | Procedure |
| 1. | Seed 200 µL of 20,000 adherent cells in culture medium in each well of a 96-well plate. The plates included in the kit are sterile and treated for cell culture. For suspension cells and loosely attached cells, coat the plates with 100 µL of 10 µg/ml Poly-L-Lysine (not included) to each well of a 96-well plate for 30 minutes at 37 °C prior to adding cells. |
| 2. | Incubate the cells for overnight at 37 °C, 5% CO2. |
| 3. | Treat the cells as desired. |
| 4. | Remove the cell culture medium and rinse with 200 µL of 1x TBS, twice. |
| 5. | Fix the cells by incubating with 100 µL of Fixing Solution for 20 minutes at room temperature. The 4% formaldehyde is used for adherent cells and 8% formaldehyde is used for suspension cells and loosely attached cells. |
| 6. | Remove the Fixing Solution and wash the plate 3 times with 200 µL 1x Wash Buffer for five minutes each time with gentle shaking on the orbital shaker. The plate can be stored at 4 °C for a week. |
| 7. | Add 100 µL of Quenching Buffer and incubate for 20 minutes at room temperature. |
| 8. | Wash the plate 3 times with 1x Wash Buffer for 5 minutes each time. |
| 9. | Add 200 µL of Blocking Buffer and incubate for 1 hour at room temperature. |
| 10. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 11. | Add 50 µL of 1x primary antibodies Anti-SF1 (Phospho-Ser82) Antibody, Anti-SF1 Antibody and/or Anti-GAPDH Antibody) to the corresponding wells, cover with Parafilm and incubate for 16 hours (overnight) at 4 °C. If the target expression is known to be high, incubate for 2 hours at room temperature. |
| 12. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 13. | Add 50 µL of 1x secondary antibodies (HRP-Conjugated AntiRabbit IgG Antibody or HRP-Conjugated Anti-Mouse IgG Antibody) to corresponding wells and incubate for 1.5 hours at room temperature. |
| 14. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 15. | Add 50 µL of Ready-to-Use Substrate to each well and incubate for 30 minutes at room temperature in the dark. |
| 16. | Add 50 µL of Stop Solution to each well and read OD at 450 nm immediately using the microplate reader. |
(Additional Crystal Violet staining may be performed if desired – details of this may be found in the kit technical manual.)
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