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HSPG Kit ELISA

HSPG Reactivité: Humain Colorimetric Sandwich ELISA 15.6 pg/mL - 1000 pg/mL Plasma, Serum, Tissue Homogenate
N° du produit ABIN6954521
  • Antigène Voir toutes HSPG Kits ELISA
    HSPG (Heparan Sulphate Protoglycans (HSPG))
    Reactivité
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    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    15.6 pg/mL - 1000 pg/mL
    Seuil minimal de détection
    15.6 pg/mL
    Application
    ELISA
    Fonction
    The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of HSPG in human serum, plasma, tissue homogenates.
    Type d'échantillon
    Plasma, Serum, Tissue Homogenate
    Analytical Method
    Quantitative
    Specificité
    This assay has high sensitivity and excellent specificity for detection of Heparan Sulfate Proteoglycan (HSPG)
    Sensibilité
    5.9 pg/mL
    Ingrédients
    • Pre-coated, ready to use 96-well strip plate, flat buttom
    • Plate sealer for 96 wells
    • Reference Standard
    • Standard Diluent
    • Detection Reagent A
    • Detection Reagent B
    • Assay Diluent A
    • Assay Diluent B
    • Reagent Diluent (if Detection Reagent is lyophilized)
    • TMB Substrate
    • Stop Solution
    • Wash Buffer (30 x concentrate)
    • Instruction manual
  • Commentaires

    Information on standard material:
    The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

    Information on reagents:
    The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

    Information on antibodies:
    The provided antibodies and their host vary in different kits.

    Volume d'échantillon
    100 μL
    Durée du test
    3 h
    Plaque
    Pre-coated
    Protocole
    1. Prepare all reagents, samples and standards,
    2. Add 100μL standard or sample to each well. Incubate 1 hours at 37 °C,
    3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37 °C,
    4. Aspirate and wash 3 times,
    5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
    6. Aspirate and wash 5 times,
    7. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
    8. Add 50μL Stop Solution. Read at 450nm immediately.
    Préparation des réactifs
    1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
    2. Standard - Reconstitute the Standard with 1.0 mL of Standard Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 1,000pg/mL. Prepare 7 tubes containing 0.5 mL Standard Diluent and produce a double dilution series. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 1,000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.2pg/mL, 15.6pg/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0pg/mL.
    3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
    4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
    5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.

    Note:

    1. Making serial dilution in the wells directly is not permitted.
    2. Prepare standards within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
    3. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
    4. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
    5. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
    6. Contaminated water or container for reagent preparation will influence the detection result.
    Préparation de l'échantillon
    • It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturationmay occur in these samples, leading to false results. Samples should therefore be stored for a short periodat 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thawcycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged toremove precipitates.
    • If the sample type is not specified in the instructions, a preliminary test is necessary to determinecompatibility with the kit.
    • If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibilityof causing a deviation due to the introduced chemical substance.The recommended dilution factor is for reference only.
    • Please estimate the concentration of the samples before performing the test. If the values are not in therange of the standard curve, the optimal sample dilution for the particular experiment has to be determined.Samples should then be diluted with PBS (pH =7.0-7.2).
    Précision du teste
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
    CV(%) = SD/meanX100
    Intra-Assay: CV < 10%
    Inter-Assay: CV < 12%
    Restrictions
    For Research Use only
  • Précaution d'utilisation
    The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    1. For unopened kit: All reagents should be stored according to the labels on the vials. The Standard, Detection Reagent A, Detection Reagent B, and 96-well Strip Plate should be stored at -20 °C upon receipt, while the other reagents should be stored at 4 °C.
    2. For opened kits: the remaining reagents must be stored according to the above storage conditions. In addition, please return the unused wells to the foil pouch containing the desiccant and seal the foil pouch with the zipper.
    .
    Date de péremption
    6 months
  • Alyoussef, Al-Gayyar: "Cytotoxic and partial hepatoprotective activity of sodium ascorbate against hepatocellular carcinoma through inhibition of sulfatase-2 in vivo and in vitro." dans: Biomedicine & pharmacotherapy, Vol. 103, pp. 362-372, (2018) (PubMed).

    Zhai, Wang, Zhang, Liang, Fu, Cui, Yang, Gong, Li, Yu, Xie, Yang, Yang, Gao: "Glioma targeting peptide modified apoferritin nanocage." dans: Drug delivery, Vol. 25, Issue 1, pp. 1013-1024, (2018) (PubMed).

    Nelson, Johansson, Tydén, Bodelsson: "Circulating syndecans during critical illness." dans: APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, Vol. 125, Issue 5, pp. 468-475, (2017) (PubMed).

    Arthur, McCall, Jolly, Kinsella, Kirk, Shelley: "Endothelial glycocalyx layer shedding following lung resection." dans: Biomarkers in medicine, Vol. 10, Issue 10, pp. 1033-1038, (2016) (PubMed).

    Jung, Fuernau, Muench, Desch, Eitel, Schuler, Adams, Figulla, Thiele: "Impairment of the endothelial glycocalyx in cardiogenic shock and its prognostic relevance." dans: Shock (Augusta, Ga.), Vol. 43, Issue 5, pp. 450-5, (2015) (PubMed).

    Tayel, Abd El Galil, Ebrahim, Ibrahim, El-Gayar, Al-Gayyar: "Suramin inhibits hepatic tissue damage in hepatocellular carcinoma through deactivation of heparanase enzyme." dans: European journal of pharmacology, Vol. 728, pp. 151-60, (2014) (PubMed).

    Al-ofi, Coffelt, Anumba: "Fibrinogen, an endogenous ligand of Toll-like receptor 4, activates monocytes in pre-eclamptic patients." dans: Journal of reproductive immunology, Vol. 103, pp. 23-8, (2014) (PubMed).

    Zaghloul, El-Shishtawy, El Galil, Ebrahim, Metwaly, Al-Gayyar: "Evaluation of antiglypican-3 therapy as a promising target for amelioration of hepatic tissue damage in hepatocellular carcinoma." dans: European journal of pharmacology, Vol. 746, pp. 353-62, (2014) (PubMed).

  • Antigène Voir toutes HSPG Kits ELISA
    HSPG (Heparan Sulphate Protoglycans (HSPG))
    Autre désignation
    Heparan Sulfate Proteoglycan (HSPG) (HSPG Produits)
    Synonymes
    CDW44 Kit ELISA, CSPG8 Kit ELISA, ECMR-III Kit ELISA, HCELL Kit ELISA, HUTCH-I Kit ELISA, IN Kit ELISA, LHR Kit ELISA, MC56 Kit ELISA, MDU2 Kit ELISA, MDU3 Kit ELISA, MIC4 Kit ELISA, Pgp1 Kit ELISA, AU023126 Kit ELISA, AW121933 Kit ELISA, AW146109 Kit ELISA, HERMES Kit ELISA, Ly-24 Kit ELISA, Pgp-1 Kit ELISA, CD44A Kit ELISA, METAA Kit ELISA, RHAMM Kit ELISA, CD44 molecule (Indian blood group) Kit ELISA, glypican 3 Kit ELISA, CD44 antigen Kit ELISA, CD44 Kit ELISA, GPC3 Kit ELISA, Cd44 Kit ELISA
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