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HSPD1 ELISA Kit

HSPD1 Reaktivität: Human Colorimetric Sandwich ELISA 1.56 ng/mL - 100 ng/mL Plasma, Serum, Tissue Homogenate
Produktnummer ABIN6974288
  • Target Alle HSPD1 ELISA Kits anzeigen
    HSPD1 (Heat Shock 60kDa Protein 1 (Chaperonin) (HSPD1))
    Reaktivität
    • 6
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Detektionsbereich
    1.56 ng/mL - 100 ng/mL
    Untere Nachweisgrenze
    1.56 ng/mL
    Applikation
    ELISA
    Verwendungszweck
    For the quantitative determination of human heat shock protein 60 (HSP-60) concentrations in serum, plasma, tissue homogenates.
    Proben
    Plasma, Serum, Tissue Homogenate
    Analytische Methode
    Quantitative
    Spezifität
    This assay has high sensitivity and excellent specificity for detection of human HSP-60. No significant cross-reactivity or interference between human HSP-60 and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between human HSP-60 and all the analogues, therefore, cross reaction may still exist.
    Sensitivität
    0.39 ng/mL
    Bestandteile
    • Assay plate
    • Standard
    • HRP-avidin (100 x concentrate)
    • Biotin-antibody (100 x concentrate)
    • Sample Diluent
    • HRP-avidin Diluent
    • Biotin-antibody Diluent
    • Wash Buffer (25 x concentrate)
    • TMB Substrate
    • Stop Solution
    • Adhesive Strip
    Top Product
    Discover our top product HSPD1 ELISA Kit
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Probenmenge
    100 μL
    Testdauer
    1 - 4.5 h
    Plattentyp
    Pre-coated
    Protokoll
    1. Prepare reagents, samples and standards as instructed.
    2. Add 100 µL standard or sample to each well. Incubate 2 hours at 37 °C.
    3. Remove the liquid of each well, don't wash.
    4. Add 100 µL Biotin-antibody (1x) to each well. Incubate 1 hour at 37 °C.
    5. Aspirate and wash 3 times.
    6. Add 100 µL HRP-avidin (1x) to each well. Incubate 1 hour at 37 °C
    7. Aspirate and wash 5 times.
    8. Add 90 μL of TMB Substrate to each well. Incubate for 15-30 minutes at 37 °C. Protect from light.
    9. Add 50 µL Stop Solution to each well. Read at 450 nm within 5 minutes.
    Aufbereitung der Reagenzien
    1. Biotin-antibody (1x) - Centrifuge the vial before opening. Biotin-antibody requires a 100-fold dilution. A suggested 100-fold dilution is 10 μL of Biotin-antibody + 990 μL of Biotin-antibody Diluent.
    2. HRP-avidin (1x) - Centrifuge the vial before opening. HRP-avidin requires a 100-fold dilution. A suggested 100-fold dilution is 10 μL of HRP-avidin + 990 μL of HRP-avidin Diluent.
    3. Wash Buffer (1x) - If crystals have formed in the concentrate, warm up to room temperature and mix gently until the crystals have completely dissolved. Dilute 20 mL of Wash Buffer Concentrate (25 x) into deionized or distilled water to prepare 500 mL of Wash Buffer (1 x).
    4. Standard Centrifuge the standard vial at 6000-10000rpm for 30s. Reconstitute the Standard with 1.0 mL of Sample Diluent. Do not substitute other diluents. This reconstitution produces a stock solution of 100 ng/mL. Mix the standard to ensure complete reconstitution and allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making dilutions. Pipette 250 μL of Sample Diluent into each tube (S0-S6). Use the stock solution to produce a 2-fold dilution series (below). Mix each tube thoroughly before the next transfer. The undiluted Standard serves as the high standard (100 ng/mL). Sample Diluent serves as the zero standard (0 ng/mL).
    Note:
    • Kindly use graduated containers to prepare the reagent. Please don't prepare the reagent directly in the Diluent vials provided in the kit.
    • Bring all reagents to room temperature (18-25 °C) before use for 30 min.
    • Prepare fresh standard for each assay. Use within 4 hours and discard after use.
    • Making serial dilution in the wells directly is not permitted.
    • Please carefully reconstitute Standards according to the instruction, and avoid foaming and mix gently until the crystals have completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10 μL for once pipetting.
    • Distilled water is recommended to be used to make the preparation for reagents. Contaminated water or container for reagent preparation will influence the detection result.
    Aufbereitung der Proben
    • 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).
    Testpräzision
    Intra-assay Precision (Precision within an assay): CV%<8% Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10% Three samples of known concentration were tested in twenty assays to assess.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Unopened kit Store at 2 - 8°C. Do not use the kit beyond the expiration date. May be stored for up to 1 month at 2 - 8°C. Coated assay Try to keep it in a sealed aluminum foil bag, plate and avoid the damp. Standard May be stored for up to 1 month at 2 - 8° C. If Biotin-antibody don't make recent use, better keep it store at HRP-avidin -20°C. Biotin-antibody Diluent Opened kit HRP-avidin Diluent Sample May be stored for up to 1 month at 2 - 8°C. Diluent Wash Buffer TMB Substrate Stop Solution *Provided this is within the expiration date of the kit.
    Haltbarkeit
    6 months
  • Sell, Poitou, Habich, Bouillot, Eckel, Clément: "Heat Shock Protein 60 in Obesity: Effect of Bariatric Surgery and its Relation to Inflammation and Cardiovascular Risk." in: Obesity (Silver Spring, Md.), Vol. 25, Issue 12, pp. 2108-2114, (2018) (PubMed).

    Roumans, Camps, Renes, Bouwman, Westerterp, Mariman: "Weight loss-induced stress in subcutaneous adipose tissue is related to weight regain." in: The British journal of nutrition, Vol. 115, Issue 5, pp. 913-20, (2016) (PubMed).

    Dolasik, Birtas Atesoglu, Tarkun, Mehtap, Keski, Dogru, Hacihanefioglu: "Decreased serum heat shock protein 60 levels in newly diagnosed immune thrombocytopenia patients." in: Platelets, Vol. 26, Issue 3, pp. 220-3, (2015) (PubMed).

    Märker, Sell, Zillessen, Glöde, Kriebel, Ouwens, Pattyn, Ruige, Famulla, Roden, Eckel, Habich: "Heat shock protein 60 as a mediator of adipose tissue inflammation and insulin resistance." in: Diabetes, Vol. 61, Issue 3, pp. 615-25, (2012) (PubMed).

    Richmond: "The John W. Knutson Distinguished Service Award in Dental Public Health--1989 recipient: John M. Frankel (posthumously)." in: Journal of public health dentistry, Vol. 50, Issue 5, pp. 345-50, (1990) (PubMed).

  • Target Alle HSPD1 ELISA Kits anzeigen
    HSPD1 (Heat Shock 60kDa Protein 1 (Chaperonin) (HSPD1))
    Andere Bezeichnung
    heat shock 60kDa protein 1 (chaperonin) (HSPD1 Produkte)
    Synonyme
    CPN60 ELISA Kit, GROEL ELISA Kit, HLD4 ELISA Kit, HSP-60 ELISA Kit, HSP60 ELISA Kit, HSP65 ELISA Kit, HuCHA60 ELISA Kit, SPG13 ELISA Kit, chaperonin ELISA Kit, cpn60 ELISA Kit, groel ELISA Kit, hld4 ELISA Kit, hsp60 ELISA Kit, hsp65 ELISA Kit, spg13 ELISA Kit, 60kDa ELISA Kit, Hsp60 ELISA Kit, 12 ELISA Kit, BP5 ELISA Kit, CG12101 ELISA Kit, Cpn60 ELISA Kit, Dmel\\CG12101 ELISA Kit, Dmhsp60 ELISA Kit, G62 ELISA Kit, HSP60A ELISA Kit, Hsp60A ELISA Kit, IEF16 ELISA Kit, Mmp-P1 ELISA Kit, SSP 7506 ELISA Kit, d-hsp60 ELISA Kit, hsp60A ELISA Kit, l(1)10Ac ELISA Kit, l(1)BP5 ELISA Kit, l(1)G8 ELISA Kit, l(1)HM21 ELISA Kit, l(1)L12 ELISA Kit, l(1)dp025 ELISA Kit, cb863 ELISA Kit, fa04a05 ELISA Kit, fb22d10 ELISA Kit, fi27b05 ELISA Kit, id:ibd2197 ELISA Kit, sb:cb144 ELISA Kit, wu:fa04a05 ELISA Kit, wu:fb22d10 ELISA Kit, wu:fi04a12 ELISA Kit, wu:fi27b05 ELISA Kit, MIF4 ELISA Kit, MNA2 ELISA Kit, mopA ELISA Kit, groL ELISA Kit, crpA ELISA Kit, Hspd1-30p ELISA Kit, heat shock protein family D (Hsp60) member 1 ELISA Kit, heat shock protein family D (Hsp60) member 1 S homeolog ELISA Kit, 60 kDa heat shock protein, mitochondrial ELISA Kit, heat shock protein 1 (chaperonin) ELISA Kit, Heat shock protein 60A ELISA Kit, heat shock 60 protein 1 ELISA Kit, chaperone ATPase HSP60 ELISA Kit, molecular chaperone GroEL ELISA Kit, thermosome subunit ELISA Kit, chaperonin GroEL ELISA Kit, mitochondrial chaperonin ELISA Kit, heat shock protein family D member 1 ELISA Kit, HSPD1 ELISA Kit, hspd1.S ELISA Kit, hspd1 ELISA Kit, LOC100414401 ELISA Kit, Hspd1 ELISA Kit, Hsp60A ELISA Kit, HSP60 ELISA Kit, groEL ELISA Kit, MMP_RS07785 ELISA Kit, groEl ELISA Kit, LOC100136430 ELISA Kit
    Hintergrund

    Abbreviation: HSPD1

    Alias: CPN60, GROEL, HLD4, HSP60, HSP65, HuCHA60, SPG13, P60 lymphocyte protein|chaperonin|heat shock protein 65|mitochondrial matrix protein P1|short heat shock protein 60 Hsp60s1

    UniProt
    P10809
    Pathways
    Activation of Innate immune Response, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity
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