HSP90 Kit ELISA

N° du produit ABIN6956432

Détail du produit HSP90 Kit ELISA

Antigène: HSP90 (Heat Shock Protein 90 (HSP90))

Reactivité: Boeuf (Vache)

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Gamme de detection: 3.12 ng/mL - 200 ng/mL

Seuil minimal de détection: 3.12 ng/mL

Application: ELISA

Fonction: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of HSP90 in bovine serum, plasma, tissue homogenates, cell lysates, cell culture supernates.

Type d'échantillon: Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate

Analytical Method: Quantitative

Specificité: This assay has high sensitivity and excellent specificity for detection of Heat Shock Protein 90 (HSP90)

Sensibilité: 1.13 ng/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

Information d'application

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 200 ng/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 200 ng/mL, 100 ng/mL, 50 ng/mL, 25 ng/mL, 12.5 ng/mL, 6.25 ng/mL, 3.12 ng/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0 ng/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

Stockage

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.

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Date de péremption: 6 months

Détail du antigène

Antigène: HSP90 (Heat Shock Protein 90 (HSP90))

Abstract: HSP90 Produits

Synonymes: EL52 Kit ELISA, HSP86 Kit ELISA, HSP89A Kit ELISA, HSP90A Kit ELISA, HSP90N Kit ELISA, HSPC1 Kit ELISA, HSPCA Kit ELISA, HSPCAL1 Kit ELISA, HSPCAL4 Kit ELISA, HSPN Kit ELISA, Hsp89 Kit ELISA, Hsp90 Kit ELISA, LAP2 Kit ELISA, git10 Kit ELISA, swo1 Kit ELISA, HSP90 Kit ELISA, htpG Kit ELISA, SCBAC25F8.08 Kit ELISA, 23.m06066 Kit ELISA, 17.m07646 Kit ELISA, HSP90-1 Kit ELISA, 143198_at Kit ELISA, 83 Kit ELISA, 83K HSP Kit ELISA, DMHSP82 Kit ELISA, E(sev)3A Kit ELISA, E(sina)2 Kit ELISA, HSP82 Kit ELISA, HSP83 Kit ELISA, ORF1 Kit ELISA, Su(Raf)3A Kit ELISA, anon-EST:Liang-2.53 Kit ELISA, anon-WO0068693 Kit ELISA, anon-WO0140519.209 Kit ELISA, clone 2.53 Kit ELISA, en(lz)3C/4C Kit ELISA, hsp84 Kit ELISA, l(3)j5C2 Kit ELISA, ms(3)08445 Kit ELISA, stc Kit ELISA, DmelCG1242 Kit ELISA, CG1242 Kit ELISA, Hsp86 Kit ELISA, Hspca Kit ELISA, 86kDa Kit ELISA, 89kDa Kit ELISA, AL024080 Kit ELISA, AL024147 Kit ELISA, Hsp86-1 Kit ELISA, hsp4 Kit ELISA, hsp86 Kit ELISA, hsp89 Kit ELISA, hsp90 Kit ELISA, hsp90a Kit ELISA, hspc1 Kit ELISA, hspca Kit ELISA, hspn Kit ELISA, lap2 Kit ELISA, Hsp90alpha Kit ELISA, heat shock protein 90 alpha family class A member 1 Kit ELISA, heat shock protein Hsp90 Kit ELISA, Hsp90 chaperone Kit ELISA, Heat shock protein 90 Kit ELISA, heat shock protein 90 Kit ELISA, chaperone protein HtpG Kit ELISA, molecular chaperone HtpG Kit ELISA, Heat Shock Protein 90 Kit ELISA, uncharacterized LOC100384473 Kit ELISA, Heat shock protein 83 Kit ELISA, heat shock protein 90, alpha (cytosolic), class A member 1 Kit ELISA, heat shock protein 90 alpha family class B member 1 Kit ELISA, heat shock protein 90kDa alpha family class A member 1 L homeolog Kit ELISA, heat shock protein HSP 90-alpha Kit ELISA, HSP90AA1 Kit ELISA, hsp90 Kit ELISA, HSP90 Kit ELISA, daf-21 Kit ELISA, htpG Kit ELISA, SCO7516 Kit ELISA, MAP_RS10510 Kit ELISA, TP04_0646 Kit ELISA, TP01_0934 Kit ELISA, APH_RS03525 Kit ELISA, GbCGDNIH1_0315 Kit ELISA, MAV_2118 Kit ELISA, HSP90C Kit ELISA, BBOV_IV008400 Kit ELISA, BBOV_III007380 Kit ELISA, ACICU_00312 Kit ELISA, ECL_01244 Kit ELISA, YE105_C1172 Kit ELISA, pco153543(105) Kit ELISA, Hsp83 Kit ELISA, Hsp90aa1 Kit ELISA, HSP90AB1 Kit ELISA, hsp90aa1.1.L Kit ELISA, LOC108698781 Kit ELISA

Pathways: M Phase, Regulation of Cell Size, Signaling Events mediated by VEGFR1 and VEGFR2, VEGFR1 Specific Signals