Description
HOXA7 Colorimetric Cell-Based ELISA
The HOXA7 Colorimetric Cell-Based ELISA Kit is specifically designed for the accurate measurement of HOXA7 levels in cell lysates and culture supernatants. This kit offers high sensitivity and specificity, allowing for precise and reproducible results for a variety of research applications.HOXA7 is a transcription factor that plays a critical role in regulating gene expression and development. Abnormalities in HOXA7 expression have been linked to various diseases, including cancer and developmental disorders.
By accurately quantifying HOXA7 levels, researchers can gain valuable insights into the molecular mechanisms underlying these conditions and potentially identify new therapeutic targets.With its easy-to-use protocol and reliable performance, the HOXA7 Colorimetric Cell-Based ELISA Kit is an essential tool for researchers studying gene expression, developmental biology, and disease mechanisms. Invest in this kit today to advance your research and uncover new discoveries in the field of molecular biology.
| Product Name: | HOXA7 Colorimetric Cell-Based ELISA |
| Product Code: | CBCAB00999 |
| ELISA Type: | Cell-Based |
| Target: | HOXA7 |
| Reactivity: | Human, Mouse, Rat |
| Dynamic Range: | > 5000 Cells |
| Detection Method: | Colorimetric 450 nmStorage/Stability:4°C/6 Months |
| Format: | 96-Well Microplate |
The HOXA7 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect HOXA7 protein expression profile in cells. The kit can be used for measuring the relative amounts of HOXA7 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on HOXA7.
Qualitative determination of HOXA7 concentration is achieved by an indirect ELISA format. In essence, HOXA7 is captured by HOXA7-specific primary antibodies while the HRP-conjugated secondary antibodies bind the Fc region of the primary antibody. Through this binding, the HRP enzyme conjugated to the secondary 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: 3204, UniProt ID: P31268, OMIM: 142950, Unigene: Hs.660918 |
| Gene Symbol: | HOXA7 |
| Sub Type: | None |
| UniProt Protein Function: | HOXA7: Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. Belongs to the Antp homeobox family. |
| UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; DNA-binding; Transcription factor Chromosomal Location of Human Ortholog: 7p15.2 Cellular Component: nucleus Molecular Function:sequence-specific DNA binding; transcription factor binding Biological Process: angiogenesis; anterior/posterior pattern formation; embryonic skeletal morphogenesis; negative regulation of cell-matrix adhesion; negative regulation of keratinocyte differentiation; negative regulation of leukocyte migration; negative regulation of monocyte differentiation; negative regulation of transcription from RNA polymerase II promoter; negative regulation of transcription, DNA-dependent; positive regulation of transcription from RNA polymerase II promoter; stem cell differentiation; transcription from RNA polymerase II promoter |
| NCBI Summary: | In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. For example, the encoded protein represses the transcription of differentiation-specific genes during keratinocyte proliferation, but this repression is then overcome by differentiation signals. This gene is highly similar to the antennapedia (Antp) gene of Drosophila. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P31268 |
| NCBI GenInfo Identifier: | 311033439 |
| NCBI Gene ID: | 3204 |
| NCBI Accession: | P31268.3 |
| UniProt Secondary Accession: | P31268,O43368, O43486, O95655, Q9NSC8, Q9UDM1, A4D191 |
| UniProt Related Accession: | P31268 |
| Molecular Weight: | 25,355 Da |
| NCBI Full Name: | Homeobox protein Hox-A7 |
| NCBI Synonym Full Names: | homeobox A7 |
| NCBI Official Symbol: | HOXA7 |
| NCBI Official Synonym Symbols: | ANTP; HOX1; HOX1A; HOX1.1 |
| NCBI Protein Information: | homeobox protein Hox-A7 |
| UniProt Protein Name: | Homeobox protein Hox-A7 |
| UniProt Synonym Protein Names: | Homeobox protein Hox 1.1; Homeobox protein Hox-1A |
| Protein Family: | Homeobox protein |
| UniProt Gene Name: | HOXA7 |
| UniProt Entry Name: | HXA7_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-HOXA7 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.)
