Hemopexin ELISA 试剂盒 (HPX)

Details for Product HPX ELISA Kit No. ABIN612795, 供应商: Log in to see
  • HPX
  • HX
  • Hpxn
  • hx
  • wu:fi17f11
  • wu:fi19a10
  • hemopexin
  • HPX
  • Mmar10_1124
  • Hpx
  • hpx

Kits with alternative reactivity to:
Competition ELISA
50 ng/mL
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原理 The AssayMax Human Hemopexin ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for detection of human hemopexin in plasma, and serum
品牌 AssayMax
样品类型 Plasma
Analytical Method Quantitative
检测方法 Colorimetric
组件 Hemopexin Microplate: A 96-well polystyrene microplate (12 strips of 8 wells) coated with a polyclonal antibody against human hemopexin. Sealing Tapes: Each kit contains 3 pre-cut, pressure-sensitive sealing tapes, which can be cut to fit the format of the individual assay. Hemopexin Standard: Human Hemopexin in a buffered protein base (5 µg, lyophilized). Biotinylated Hemopexin: 1 vial, lyophilized. MIx Diluent Concentrate (10x): A 10-fold concentrated buffered protein base (30 ml). 1 Wash Buffer Concentrate (20x): A 20-fold concentrated buffered surfactant (30 ml). Streptavidin-Peroxidase Conjugate (SP Conjugate): A 100-fold concentrate (90µl). 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 450 nm. Pipettes (1-20 µL, 20-200 µL, 200-1000µLand multiple channel). Deionized or distilled reagent grade water.
Plasmids, Primers & others Plasmids, Primers & others Hemopexin products on genomics-online (e.g. as negative or positive controls)
别名 Hemopexin (HPX ELISA Kit 摘要)
背景 Hemopexin is a heme-binding plasma glycoprotein which, after haptoglobin, forms the second line of defense against hemoglobin-mediated oxidative damage during intravascular hemolysis. A decrease in plasma hemopexin concentration reflects a recent release of heme compounds in the extracellular compartment. Heme-hemopexin complexes are delivered to hepatocytes by receptor-mediated endocytosis after which hemopexin is recycled to the circulation. Studies indicated that increased hemopexin level associate with minimal change disease (MCD) , sporadic Alzheimer's disease (AD) , heavy-drinking chronic alcoholics , hemolytic anemias, chronic neuromuscular diseases and acute intermittent porphyria.
途径 Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response
样本量 25 μL
实验时间 < 2 h
板类型 Pre-coated
实验流程 This assay employs a quantitative competitive enzyme immunoassay technique that measures human hemopexin in less than 2 hours. A polyclonal antibody specific for human hemopexin has been pre-coated onto a 96-well microplate with removable strips. Hemopexin in standards and samples is competed by a biotinylated hemopexin sandwiched by the immobilized antibody and streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.

Freshly dilute all reagents and bring all reagents to room temperature before use. If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved. MIx Diluent Concentrate (10x): Dilute the MIx Diluent 1:10 with reagent grade water. Store for up to 1 month at 2-8°C. Standard Curve: Reconstitute the 5 g of Hemopexin Standard with 1 ml of MIx Diluent to generate a solution of 5 g/ml. Allow the standard to sit for 10 minutes with gentle agitation prior to making dilutions. Prepare triplicate standard points by serially diluting the standard solution (5 g/ml) 1:4 with MIx Diluent to produce 1.25, 0.313 and 0.078 g/ml solutions. MIx Diluent serves as the zero standard (0 g/ml). Any remaining solution should be frozen at -20°C. Standard Point Dilution [Hemopexin] ( g/ml) Standard (5 g/ml) P1 5.000 P2 1 part P1 + 3 parts MIx Diluent 1.250 P3 1 part P2 + 3 parts MIx Diluent 0.313 P4 1 part P3 + 3 parts MIx Diluent 0.078 P5 MIx Diluent 0.000 Biotinylated Hemopexin (2x): Dilute Biotinylated Hemopexin with 4 ml MIx Diluent to produce to stock solution. Allow to sit for 10 minutes with gentle agitation prior to making dilutions. The stock solution should be further diluted 1:2 with MIx Diluent. Any remaining solution should be frozen at -20°C. Wash Buffer Concentrate (20x): Dilute the Wash Buffer Concentrate 1:20 with reagent grade water. SP Conjugate (100x): Spin down the SP Conjugate briefly and dilute the desired amount of the conjugate 1:100 with MIx Diluent. Any remaining solution should be frozen at -20°C.

样品收集 Plasma: Collect plasma using one-tenth volume of 0.1 M sodium citrate as an anticoagulant. Centrifuge samples at 2000 x g for 10 minutes and assay. Dilute samples 1:400 into MIx Diluent. Store samples 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 2000 x g for 10 minutes. Remove serum and assay. Dilute samples 1:400 into MIx Diluent. Store serum at -20°C or below. Avoid repeated freeze-thaw cycles.

Prepare all reagents, working standards and samples as instructed. Bring all reagents to room temperature before use. The assay is performed at room temperature (20 - 30 °C). Remove excess microplate strips from the plate frame and return them immediately to the foil pouch with desiccant inside. Reseal the pouch securely to minimize exposure to water vapor and store in a vacuum desiccator. Add 25 µL of standard or sample per well, and immediately add 25 µL of Biotinylated Hemopexin to each well (on top of the Standard or sample) and mix gently. Cover wells with a sealing tape and incubate for one hour. Start the timer after the last sample addition. Wash five times with 200 µL of Wash Buffer. Invert the plate and decant the contents, and hit it 4-5 times on absorbent paper towel to complete remove liquid at each step. Add 50 µL of Streptavidin-Peroxidase Conjugate to each well and incubate for 30 minutes. Turn on the microplate reader and set up the program in advance. Wash five times with 200 µL of Wash Buffer. Add 50 µL of Chromogen Substrate per well and incubate for about 10 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 µL 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. Please note that after the reaction is stopped for about 10 minutes, some black particles may be generated at high concentration point, which will reduce the readings.


Calculate the mean value of the duplicate or triplicate readings for each standard and sample and subtract the mean value of zero standard readings. To generate a Standard Curve, plot the graph using the standard concentrations on the x-axis and the corresponding mean 450 nm absorbance 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. Standard Curve The curve is provided for illustration only. A standard curve should be generated each time the assay is performed.

实验精密度 Intra-assay and inter-assay coefficients of variation were 5.0% and 7.7% respectively.
限制 仅限研究用
注意事项 The kit should not be used beyond the expiration date.
储存条件 4 °C/-20 °C
储存方法 Store kit at 2-8°C or -20°C upon arrival up to the expiration date. Opened MIx Diluent may be stored for up to 1 month at 2-8°C. Store reconstituted reagents at -20°C or below. Opened unused strip wells may return to the foil pouch with the desiccant pack, reseal along zip-seal. May be stored for up to 1 month in a vacuum desiccator.
ELISA image for Hemopexin (HPX) ELISA Kit (ABIN612795) Hemopexin (HPX) ELISA Kit
有引用在: Kobayashi, Nouso, Kinugasa, Takeuchi, Tomoda, Miyahara, Hagihara, Kuwaki, Onishi, Nakamura, Ikeda, Miyake, Shiraha, Takaki, Yamamoto: "Clinical utility of serum fucosylated hemopexin in Japanese patients with hepatocellular carcinoma." in: Hepatology research : the official journal of the Japan Society of Hepatology, 2012 (PubMed).

背景 Kristensson-Aas, Wallerstedt, Alling, Cederblad, Magnusson: "Haematological findings in chronic alcoholics after heavy drinking with special reference to haemolysis." in: European journal of clinical investigation, Vol. 16, Issue 2, pp. 178-83, 1986 (PubMed).