HSPD1 ELISA Kit

Catalog No. ABIN6963528

Product Details HSPD1 ELISA Kit

Target: HSPD1 (Heat Shock 60kDa Protein 1 (Chaperonin) (HSPD1))

Reactivity: Human

Detection Method: Colorimetric

Method Type: Sandwich ELISA

Detection Range: 1.56 ng/mL - 100 ng/mL

Minimum Detection Limit: 1.56 ng/mL

Application: ELISA

Purpose: The kit is a sandwich enzyme immunoassay technique for the in vitro quantitative measurement in various sample types.

Sample Type: Cell Culture Supernatant, Plasma, Serum

Analytical Method: Quantitative

Specificity: This kit recognizes Human HSP-60/HSPD1 in samples. No Significant cross-reactivity or interference between Human HSP-60/HSPD1 and analogues was observed.

Sensitivity: 0.94 ng/mL

Components:

• Pre-coated, ready to use 96-well strip plate, flat buttom
• Plate sealer for 96 wells
• Reference Standard
• Reference Standard & Sample Diluent
• Biotinylated Detection Antibody (100 x concentrate)
• HRP Conjugate (100 x concentrate)
• Biotinylated Detection Antibody Diluent
• HRP Conjugate Diluent
• Substrate Reagent
• Stop Solution
• Wash Buffer (25 x concentrate)
• Instruction manual

Application Details

Sample Volume: 100 μL

Assay Time: 3.5 h

Plate: Pre-coated

Protocol:

1. Add 100 µL standard or sample to each well. Incubate for 90 min at 37 °C.
2. Remove the liquid. Add 100 µL Biotinylated Detection Antibody. Incubate for 1 hour at 37 °C.
3. Aspirate and wash 3 times.
4. Add 100 µL HRP Conjugate. Incubate for 30 min at 37 °C.
5. Aspirate and wash 5 times.
6. Add 90 µL Substrate Reagent. Incubate for 15 min at 37 °C.
7. Add 50 µL Stop Solution. Read at 450 nm immediately.
8. Calculation of results.

Reagent Preparation:

1. Bring all reagents to room temperature (18~25 °C) before use. Follow the Microplate reader manual for set-up and preheat it for 15 min before OD measurement.
2. Wash Buffer: Dilute 30 mL of Concentrated Wash Buffer with 720 mL of deionized or distilled water to prepare 750 mL of Wash Buffer.Note: if crystals have formed in the concentrate, warm it in a 40 °C water bath and mix it gently until the crystals have completely dissolved
3. Standard working solution: Centrifuge the standard at 10,000xg for 1 min. Add 1.0 mL of Reference Standard &Sample Diluent, let it stand for 10 min and invert it gently several times. After it dissolves fully, mix it thoroughly with a pipette. This reconstitution produces a working solution of 100 ng/mL. Then make serial dilutions as needed. The recommended dilution gradient is as follows: 100, 50, 25, 12.5, 6.25, 3.13, 1.56, 0 ng/mL. Dilution method: Take 7 EP tubes, add 500 μLof Reference Standard & Sample Diluent to each tube. Pipette 500 μLof the 100 ng/mL working solution to the first tube and mix up to produce a 50 ng/mL working solution. Pipette 500 μLof the solution from the former tube into the latter one according to these steps. The illustration below is for reference. Note: the last tube is regarded as a blank. Don't pipette solution into it from the former tube.
4. Biotinylated Detection Antibody working solution: Calculate the required amount before the experiment (100 μL/well). In preparation, slightly more than calculated should be prepared. Centrifuge the stock tube before use, dilute the 100x Concentrated Biotinylated Detection Antibody to 1xworking solution with Biotinylated Detection Antibody Diluent.
5. Concentrated HRP Conjugate working solution: Calculate the required amount before the experiment (100 μL/well). In preparation, slightly more than calculated should be prepared. Dilute the 100x Concentrated HRP Conjugate to 1x working solution with Concentrated HRP Conjugate Diluent.

Sample Preparation:

• It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturation may occur in these samples, leading to false results. Samples should therefore be stored for a short period at 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thaw cycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged to remove precipitates.
• If the sample type is not specified in the instructions, a preliminary test is necessary to determine compatibility with the kit.
• If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibility of 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 the range of the standard curve, the optimal sample dilution for the particular experiment has to be determined.

Assay Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Human HSP-60/HSPD1 were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Human HSP-60/HSPD1 were tested on 3 different plates, 20 replicates in each plate.
Both intra-CV and inter-CV are < 10 %.

Restrictions: For Research Use only

Handling

Storage: 4 °C,-20 °C

Storage Comment:

1. For unopened kit: All reagents should be stored according to the labels on the vials, so they are stable up to 12 months after receipt of the kit. The Reference Standard, Biotinylated Detection Antibody, HRP Conjugate and the 96-well stripe plate should be stored at -20 °C upon receipt while the other reagents should be stored at 4 °C.
2. For used kit: When the kit is used, the remaining reagents need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and zip-seal the foil pouch.

Expiry Date: 12 months

References for HSPD1 ELISA Kit (ABIN6963528)

Shaker, Al-Amran, Fatima, Al-Aubaid, Hadi: "Trimetazidine Improves the Outcome of EECP Therapy in Patients with Refractory Angina Pectoris." in: Medical archives (Sarajevo, Bosnia and Herzegovina), Vol. 74, Issue 3, pp. 199-204, (2020) (PubMed).

Target Details for HSPD1

Target: HSPD1 (Heat Shock 60kDa Protein 1 (Chaperonin) (HSPD1))

Alternative Name: Heat Shock Protein 60 (HSPD1 Products)

Synonyms: 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

Background: HSPD1, CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13

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