Description
Rat TGFB3/TGF-beta 3 ELISA Kit
The Rat TGFB3 (TGF Beta-3) ELISA Kit is specifically designed for the precise measurement of TGFB3 levels in rat serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring accurate and consistent results for various research purposes.TGFB3, also known as Transforming Growth Factor Beta-3, is a critical regulator of cell growth, differentiation, and development. It plays a crucial role in various biological processes, including immune response, wound healing, and tissue repair.
Dysregulation of TGFB3 has been associated with various diseases, such as cancer, fibrosis, and autoimmune disorders, highlighting its importance as a potential therapeutic target.With its reliability and versatility, the Rat TGFB3 ELISA Kit is an invaluable tool for studying the role of TGFB3 in physiological and pathological conditions, advancing our understanding of disease mechanisms, and identifying novel treatment strategies.
| Product Name: | Rat TGFB3/TGF-beta 3 ELISA Kit |
| Product Code: | RTFI00049 |
| Size: | 96 Assays |
| Target: | Rat TGF-beta3 |
| Alias: | TGF-beta3, Transforming Growth Factor Beta 3, TGFbeta3, TGFB3, ARVD, TGF-beta3, TGF-beta-3, transforming growth factor beta-3, transforming growth factor, beta 3 |
| Reactivity: | Rat |
| Detection Method: | Sandwich ELISA, Double Antibody |
| Sensitivity: | 9.375pg/ml |
| Range: | 15.625-1000pg/ml |
| Storage: | 4°C for 6 months |
| Note: | For Research Use Only |
| Recovery: | Matrices listed below were spiked with certain level of Rat TGF-beta3 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat TGF-beta3 in samples. | ||||||||||||||||
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| Linearity: | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat TGF-beta3 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% |
| Uniprot: | Q07258 |
| UniProt Protein Function: | TGFB3: Involved in embryogenesis and cell differentiation |
| UniProt Protein Details: | Protein type:Cell development/differentiation; Ligand, receptor tyrosine kinase; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide Cellular Component: cell soma; cell surface; cytoplasm; extracellular matrix; extracellular space; nucleus; proteinaceous extracellular matrix; secretory granule; T-tubule Molecular Function:cytokine activity; identical protein binding; protein heterodimerization activity; punt binding; transforming growth factor beta binding; transforming growth factor beta receptor binding Biological Process: activation of MAPK activity; aging; alveolus development; cell development; embryonic neurocranium morphogenesis; female pregnancy; gut development; in utero embryonic development; inner ear development; intercellular junction assembly and maintenance; mammary gland development; negative regulation of cell proliferation; negative regulation of DNA replication; negative regulation of neuron apoptosis; negative regulation of transforming growth factor beta receptor signaling pathway; organ morphogenesis; palate development; positive regulation of apoptosis; positive regulation of bone mineralization; positive regulation of collagen biosynthetic process; positive regulation of DNA replication; positive regulation of filopodium formation; positive regulation of protein secretion; positive regulation of transcription from RNA polymerase II promoter; positive regulation of transcription, DNA-dependent; regulation of endothelial cell differentiation; regulation of epithelial cell differentiation; regulation of epithelial cell proliferation; response to estrogen stimulus; response to hypoxia; response to progesterone stimulus; salivary gland morphogenesis; SMAD protein nuclear translocation; transforming growth factor beta receptor signaling pathway; wound healing |
| NCBI Summary: | involved in epithelial and endothelial cell proliferation and differentiation during development [RGD, Feb 2006] |
| UniProt Code: | Q07258 |
| NCBI GenInfo Identifier: | 1351228 |
| NCBI Gene ID: | 25717 |
| NCBI Accession: | Q07258.2 |
| UniProt Secondary Accession: | Q07258,Q56A31, |
| UniProt Related Accession: | Q07258 |
| Molecular Weight: | 47,116 Da |
| NCBI Full Name: | Transforming growth factor beta-3 |
| NCBI Synonym Full Names: | transforming growth factor, beta 3 |
| NCBI Official Symbol: | Tgfb3Â Â |
| NCBI Official Synonym Symbols: | TGF-B3Â Â |
| NCBI Protein Information: | transforming growth factor beta-3; TGF-beta-3 |
| UniProt Protein Name: | Transforming growth factor beta-3 |
| Protein Family: | Transforming growth factor |
| UniProt Gene Name: | Tgfb3Â Â |
| UniProt Entry Name: | TGFB3_RAT |
| 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 clotovernight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Removeserum 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 anti-coagulant. 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 & homogenizein 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. |
