GAL4 ELISA 试剂盒
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- 抗原 See all GAL4 (LGALS4) ELISA试剂盒
- GAL4 (LGALS4) (Galectin 4 (LGALS4))
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适用
- 人
- 检测方法
- Colorimetric
- 实验类型
- Sandwich ELISA
- 检测范围
- 0.0781-5 ng/mL
- 最低检测浓度
- 0.0781 ng/mL
- 应用范围
- ELISA
- 原理
- The AssayMax™ Human Galectin-4 (Gal-4) ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for detection of human galectin-4 in plasma, serum, and cell culture samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures human galectin-4 in less than 4 hours. A polyclonal antibody specific for human galectin-4 has been pre-coated onto a 96-well microplate with removable strips. Galectin-4 in standards and samples is sandwiched by the immobilized antibody and the biotinylated polyclonal antibody specific for galectin-4, which is recognized by a streptavidin-peroxidase conjugate. All unbound material is washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.
- 品牌
- AssayMax™
- 样品类型
- Cell Culture Cells, Plasma, Serum
- Analytical Method
- Quantitative
- 组件
- Human Galectin-4 Microplate: A 96-well polystyrene microplate (12 strips of 8 wells) coated with a polyclonal antibody against human galectin-4. Sealing Tapes: Each kit contains 3 precut, pressure sensitive sealing tapes that can be cut to fit the format of the individual assay. Human Galectin-4 Standard: Human galectin-4 in a buffered protein base (5 ng, lyophilized). Biotinylated Human Galectin-4 Antibody (50x): A 50-fold concentrated biotinylated polyclonal antibody against galectin-4 (120 l). MIX Diluent Concentrate (10x): A 10-fold concentrated buffered protein base (30 ml). Wash Buffer Concentrate (20x): A 20-fold concentrated buffered surfactant (30 ml, 2 bottles). Streptavidin-Peroxidase Conjugate (SP Conjugate): A 100-fold concentrate (80 l). Chromogen Substrate: A ready-to-use stabilized peroxidase chromogen substrate tetramethylbenzidine (8 ml). Stop Solution: A 0.5 N hydrochloric acid to stop the chromogen substrate reaction (12 ml).
- 试剂未包括
- Microplate reader capable of measuring absorbance at 405 nm. Pipettes (1-20 µL, 20-200 µL, and multiple channel). Deionized or distilled reagent grade water Incubator (37 °C)
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- Discover our best selling LGALS4 ELISA Kit
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- Discover our top product LGALS4 ELISA Kit
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Galectin 4 (LGALS4) ELISA Kit
LGALS4 适用: 小鼠 Colorimetric Sandwich ELISA 0.156 ng/mL - 10 ng/mL Plasma, Serum, Tissue Homogenate
Galectin 4 (LGALS4) ELISA KitLGALS4 适用: 人 Colorimetric Sandwich ELISA 62.5 pg/mL - 4000 pg/mL Plasma, Serum, Tissue Homogenate
Galectin 4 (LGALS4) ELISA KitLGALS4 适用: 大鼠 Colorimetric Sandwich ELISA 0.31 ng/mL - 20 ng/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Galectin 4 (LGALS4) ELISA KitLGALS4 适用: 人 AA 2-323 Colorimetric Sandwich ELISA 156-10.000 pg/mL Cell Culture Supernatant, Plasma (EDTA), Plasma (heparin), Serum
Galectin 4 (LGALS4) ELISA KitLGALS4 适用: 小鼠 Colorimetric Sandwich ELISA 0.156 ng/mL - 10 ng/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Galectin 4 (LGALS4) ELISA KitLGALS4 适用: 人 Colorimetric Sandwich ELISA 156-10000 pg/mL Cell Culture Supernatant, Plasma, Serum
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- 实验时间
- 4 h
- 板类型
- Pre-coated
- 实验流程
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- Step 1. Add 50 μL of Standard or Sample per well. Incubate 2 hours.
- Step 2. Wash, then add 50 μL of Biotinylated Antibody per well. Incubate 1 hour.
- Step 3. Wash, then add 50 μL of SP Conjugate per well. Incubate 30 minutes.
- Step 4. Wash, then add 50 μL of Chromogen Substrate per well. Incubate 25 minutes.
- Step 5. Add 50 μL of Stop Solution per well. Read at 450 nm immediately.
- 试剂准备
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Freshly dilute all reagents and bring all reagents to room temperature before use. MIX Diluent Concentrate (10x): If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved. Dilute the MIX Diluent Concentrate 1:10 with reagent grade water. Store for up to 30 days at 2-8 °C.
- 样品收集
- Plasma: Collect plasma using one-tenth volume of 0.1 M sodium citrate as an anticoagulant. Centrifuge samples at 3000 x g for 10 minutes, and assay. The undiluted samples can be stored at -20 °C or below for up to 3 months. Avoid repeated freeze-thaw cycles (EDTA or Heparin can also be used as anticoagulant). Serum: Samples should be collected into a serum separator tube. After clot formation, centrifuge samples at 3000 x g for 10 minutes, remove serum, and assay. The undiluted samples can be stored at -20 °C or below for up to 3 months. Avoid repeated freeze-thaw cycles. Cell Culture Supernatants: Centrifuge cell culture media at 3000 x g for 10 minutes to remove debris. Collect supernatants and assay. Store the remaining samples at -20 °C or below. Avoid repeated freeze-thaw cycles.
- 实验流程
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Prepare all reagents, standard solutions, and samples as instructed. Bring all reagents to room temperature before use. The assay is performed at room temperature (20-25 °C). Remove excess microplate strips from the plate frame and return them immediately to the foil pouch with desiccants inside. Reseal the pouch securely to minimize exposure to water vapor and store in a vacuum desiccator. Add 50 l of Human Galectin-4 Standard or sample per well. Cover wells with a sealing tape and incubate for 2 hours. Start the timer after the last addition. Wash five times with 200 l of Wash Buffer manually. Invert the plate each time and decant the contents, hit 4-5 times on absorbent material to completely remove the liquid. If using a machine, wash six times with 300 l of Wash Buffer and then invert the plate, decanting the contents, hit 4-5 times on absorbent material to completely remove the liquid. Add 50 l of Biotinylated Human Galectin-4 Antibody to each well and incubate for 1 hour. Wash the microplate as described above. Add 50 l of Streptavidin-Peroxidase Conjugate to each well and incubate for 30 minutes. Turn on the microplate reader and set up the program in advance. 5 Wash the microplate as described above. Add 50 l of Chromogen Substrate per well and incubate for 25 minutes or till the optimal blue color density develops. Gently tap plate to ensure thorough mixing and break the bubbles in the well with pipette tip. Add 50 l of Stop Solution to each well. The color will change from blue to yellow. Read the absorbance on a microplate reader at a wavelength of 450 nm immediately. If wavelength correction is available, subtract readings at 570 nm from those at 450 nm to correct optical imperfections. Otherwise, read the plate at 450 nm only. Please note that some unstable black particles may be generated at high concentration points after stopping the reaction for about 10 minutes, which will reduce the readings.
- 结果分析
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- Calculate the mean value of the duplicate or triplicate readings for each standard and sample.
- To generate a standard curve, plot the graph using the standard concentrations on the x-axis and the corresponding mean 450 nm absorbance (OD) on the y-axis. The best-fit line can be determined by regression analysis using log-log or four-parameter logistic curve-fit.
- Determine the unknown sample concentration from the standard curve and multiply the value by the dilution factor.
- 限制
- 仅限研究用
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- 注意事项
- This product is for Research Use Only and is not intended for use in diagnostic procedures. Prepare all reagents (working diluent buffer, wash buffer, standard, biotinylated antibody, and SP conjugate) as instructed, prior to running the assay. 2 Prepare all samples prior to running the assay. The dilution factors for the samples are suggested in this insert. However, the user should determine the optimal dilution factor. Spin down the SP conjugate vial and the biotinylated antibody vial before opening and using contents. The Stop Solution is an acidic solution. The kit should not be used beyond the expiration date.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Upon arrival, immediately store components of the kit at recommended temperatures up to the expiration date. Store SP Conjugate and Biotinylated Antibody at -20°C. Store Microplate, Diluent Concentrate (10x), Wash Buffer, Stop Solution, and Chromogen Substrate at 2-8°C. Unused microplate wells may be returned to the foil pouch with the desiccant packs and resealed. May be stored for up to 30 days in a vacuum desiccator. Diluent (1x) may be stored for up to 30 days at 2-8°C. Store Standard at 2-8°C before reconstituting with Diluent and at -20°C after reconstituting with Diluent. 3
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- 抗原 See all GAL4 (LGALS4) ELISA试剂盒
- GAL4 (LGALS4) (Galectin 4 (LGALS4))
- 别名
- Galectin-4 (Gal-4) (LGALS4 产品)
- 别名
- LGALS4 ELISA Kit, gal4 ELISA Kit, l36lbp ELISA Kit, MGC86186 ELISA Kit, galectin-4 ELISA Kit, xgalectin-VIa ELISA Kit, gal-4 ELISA Kit, L36LBP ELISA Kit, L-36 ELISA Kit, L36LBI ELISA Kit, GAL4 ELISA Kit, galectin 4 ELISA Kit, lectin, galactoside-binding, soluble, 4 L homeolog ELISA Kit, Galectin-4 ELISA Kit, lectin, galactose binding, soluble 4 ELISA Kit, LGALS4 ELISA Kit, lgals4.L ELISA Kit, leg4 ELISA Kit, Lgals4 ELISA Kit
- 背景
- Galectin-4 (Gal-4), also known as antigen NY-CO-27, L-36 lactose-binding protein, L36LBP, lactose-binding lectin 4 and LGALS4, is a member of the tandem-repeat-type galectin family of beta-galactoside-binding proteins. This 36-kD protein comprises 323 amino acids and contains two homologous but distinct carbohydrate-binding domains, connected by a variable-length linker region that is susceptible to proteolytic degradation (1-2). Gal-4 is able to cross-link combinations of sulfated glycosphingolipids, sulfated cholesterol, N- and O-glycosylated proteins and blood group antigens to stabilize the lipid raft and to deliver glycoproteins to the lipid rafts (3). It plays roles in cell-cell interactions, cell adhesion to extracellular matrix, tissue remodeling, growth regulation, inflammation and metastasis (4-5).
- 基因ID
- 3960
- UniProt
- P56470
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