FGF9 ELISA 试剂盒
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- 抗原 See all FGF9 (FGF-9) ELISA试剂盒
- FGF9 (FGF-9) (Fibroblast Growth Factor 9 (FGF-9))
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适用
- 人
- 检测方法
- Colorimetric
- 实验类型
- Sandwich ELISA
- 检测范围
- 62.5-4000 pg/mL
- 最低检测浓度
- 62.5 pg/mL
- 应用范围
- ELISA
- 原理
- For quantitative detection of FGF9 in human serum, plasma, body fluids, tissue lysates or cell culture supernates.
- 样品类型
- Cell Culture Supernatant, Plasma, Serum, Tissue Lysate
- Analytical Method
- Quantitative
- 灵敏度
- < 15 pg/mL
- 组件
- 1. One 96-well plate pre-coated with anti-human FGF9 antibody 2. Lyophilized FGF9 standards: 2 tubes (10ng / tube) 3. Sample / Standard diluent buffer: 30ml 4. Biotin conjugated anti-Human FGF9 antibody (Concentrated): 130 µl.
- 试剂未包括
- 1. 37 °C incubator 2. Microplate reader (wavelength: 450nm) 3. Precise pipette and disposable pipette tips 4. Automated plate washer 5. ELISA shaker 6. 1.5ml of Eppendorf tubes 7. Plate cover 8. Absorbent filter papers 9. Plastic or glass container with volume of above 1L
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- Discover our best selling FGF-9 ELISA Kit
- Top Product
- Discover our top product FGF-9 ELISA Kit
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Fibroblast Growth Factor 9 (FGF-9) ELISA Kit
FGF-9 适用: 小鼠 Colorimetric Sandwich ELISA 15.6 pg/mL - 1000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Fibroblast Growth Factor 9 (FGF-9) ELISA KitFGF-9 适用: 人 Colorimetric Sandwich ELISA 15.6 pg/mL - 1000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Fibroblast Growth Factor 9 (FGF-9) ELISA KitFGF-9 适用: 大鼠 Colorimetric Sandwich ELISA 15.6 pg/mL - 1000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Fibroblast Growth Factor 9 (FGF-9) ELISA KitFGF-9 适用: 小鸡 Colorimetric Sandwich ELISA 78.12 pg/mL - 5000 pg/mL Plasma, Serum
Fibroblast Growth Factor 9 (FGF-9) ELISA KitFGF-9 适用: Cow Colorimetric Sandwich ELISA 62.5 pg/mL - 4000 pg/mL Plasma, Serum
Fibroblast Growth Factor 9 (FGF-9) ELISA KitSmall Sample FGF-9 适用: 小鼠 Colorimetric Sandwich ELISA 15.6 pg/mL - 1000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Fibroblast Growth Factor 9 (FGF-9) ELISA KitFGF-9 适用: 人 Colorimetric Sandwich ELISA 15.6 pg/mL - 1000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Fibroblast Growth Factor 9 (FGF-9) ELISA KitFGF-9 适用: 人 Colorimetric Sandwich ELISA 62.5-4000 pg/mL Cell Culture Supernatant, Plasma, Serum
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- 说明
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This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti- FGF9 polyclonal antibody was pre-coated onto 96-well plates. And the biotin conjugated anti- FGF9 polyclonal antibody was used as detection antibodies. The standards test samples and biotin conjugated detection antibody were added - the wells subsequently and wash with wash buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with wash buffer. TMB substrates were used - visualize HRP enzymatic reaction. TMB was catalyzed by HRP - produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional - the FGF9 amount of sample captured in plate. Read the O.D. absorbance at 450 nm in a microplate reader and then the concentration of FGF9 can be calculated.
- 板类型
- Pre-coated
- 试剂准备
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- Before the experiment, centrifuge each kit component for several minutes to bring down all reagents to the bottom of tubes. 2. It is recommend to measure each standard and sample in duplicate. 3. Do NOT let the plate completely dry at any time! Since the dry condition can inactivate the biological material on the plate. 4. Do not reuse pipette tips and tubes to avoid cross contamination. 5. Do not use the expired components and the components from different batches. 6. To avoid the marginal effect of plate incubation for temperature differences (the marginal wells always get stronger reaction), it is recommend to equilibrate the ABC working solution and TMB substrate for at least 30 min at room temperature (37°C ) before adding to wells.The TMB substrate (Kit Component 8) is colorless and transparent before use, if not, please contact us for replacement.
- 样品制备
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Preparation of sample and reagents 1. Sample Isolate the test samples soon after collecting, then, analyze immediately (within 2 hours). Or aliquot and store at -20 °C for long term. Avoid multiple freeze-thaw cycles.
Tissue lysate or body fluids, cell culture supernate: Centrifuge to remove precipitate, analyze immediately or aliquot and store at -20 °C .
Serum: Coagulate the serum at room temperature (about 4 hours). Centrifuge at approximately 1000 × g for 15 min. Analyze the serum immediately or aliquot and store at -70 .° C
Plasma: Collect plasma with EDTA as the anticoagulant. Centrifuge for 15 min at 1000 x g within 30 min of collection. Analyze immediately or aliquot and store frozen at -20 °C. Heparin and citrate can not be used as anticoagulant here. Note: 1. Coagulate blood samples completely, then, centrifuge, and avoid hemolysis and particle. 2. NaN3 can not be used as test sample preservative, since it is the inhibitor for HRP. - 限制
- 仅限研究用
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- 储存液
- Sodium azide, Thimerosal (Merthiolate)
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- 抗原 See all FGF9 (FGF-9) ELISA试剂盒
- FGF9 (FGF-9) (Fibroblast Growth Factor 9 (FGF-9))
- 别名
- FGF-9 (FGF-9 产品)
- 别名
- Eks ELISA Kit, FGF-9 ELISA Kit, GAF ELISA Kit, HBFG-9 ELISA Kit, HBGF-9 ELISA Kit, SYNS3 ELISA Kit, XFGF-9 ELISA Kit, fgf9-A ELISA Kit, fibroblast growth factor 9 ELISA Kit, fibroblast growth factor 9 S homeolog ELISA Kit, Fgf9 ELISA Kit, FGF9 ELISA Kit, fgf9.S ELISA Kit
- 背景
- FGF9 is a Member of the fibroblast growth factor (FGF) gene family, FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. FGF9 was isolated as a secreted factor that exhibits a growth-stimulating effect on cultured glial cells. Its gene contains 3 exons and mapped to chromosome 13q12.11. In nervous system, this protein is produced mainly by neurons and may be important for glial cell development. FGF9 is an abundant secreted growth factor that can act as both a paracrine mitogen for epithelial cells and an autocrine mitogen for stromal cells. Overexpression of this paracrine and autocrine growth factor may play an important role in the epithelial and stromal proliferation in benign prostatic hyperplasia.
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