GFAP Kit ELISA

N° du produit ABIN6574132

Détail du produit GFAP Kit ELISA

Antigène: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Reactivité: Rat

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Gamme de detection: 62.5 pg/mL - 4000 pg/mL

Seuil minimal de détection: 62.5 pg/mL

Application: ELISA

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

We offer validation data (WB) for the kit components. So you can be sure to order a reliable ELISA kit product composed of high quality reagents.

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 Glial Fibrillary Acidic Protein (GFAP)

Réactivité croisée (Details): No significant cross-reactivity or interference between Glial Fibrillary Acidic Protein (GFAP) and analogues was observed.

Sensibilité: 26.1 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

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 4,000pg/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 4,000pg/mL, 2,000pg/mL, 1,000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/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

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

Références pour GFAP Kit ELISA (ABIN6574132)

Mirahmadi, Shahmohammadi, Rousta, Azadi, Fahanik-Babaei, Baluchnejadmojarad, Roghani: "Soy isoflavone genistein attenuates lipopolysaccharide-induced cognitive impairments in the rat via exerting anti-oxidative and anti-inflammatory effects." dans: Cytokine, Vol. 104, pp. 151-159, (2018) (PubMed).

Baluchnejadmojarad, Eftekhari, Jamali-Raeufy, Haghani, Zeinali, Roghani: "The anti-aging protein klotho alleviates injury of nigrostriatal dopaminergic pathway in 6-hydroxydopamine rat model of Parkinson's disease: Involvement of PKA/CaMKII/CREB signaling." dans: Experimental gerontology, Vol. 100, pp. 70-76, (2018) (PubMed).

Afshin-Majd, Bashiri, Kiasalari, Baluchnejadmojarad, Sedaghat, Roghani: "Acetyl-l-carnitine protects dopaminergic nigrostriatal pathway in 6-hydroxydopamine-induced model of Parkinson's disease in the rat." dans: Biomedicine & pharmacotherapy, Vol. 89, pp. 1-9, (2017) (PubMed).

Baluchnejadmojarad, Jamali-Raeufy, Zabihnejad, Rabiee, Roghani: "Troxerutin exerts neuroprotection in 6-hydroxydopamine lesion rat model of Parkinson's disease: Possible involvement of PI3K/ERβ signaling." dans: European journal of pharmacology, Vol. 801, pp. 72-78, (2017) (PubMed).

Sedaghat, Taab, Kiasalari, Afshin-Majd, Baluchnejadmojarad, Roghani: "Berberine ameliorates intrahippocampal kainate-induced status epilepticus and consequent epileptogenic process in the rat: Underlying mechanisms." dans: Biomedicine & pharmacotherapy, Vol. 87, pp. 200-208, (2017) (PubMed).

Abdel-Hamid, Firgany, Ali: "Effect of memantine: A NMDA receptor blocker, on ethambutol-induced retinal injury." dans: Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft, Vol. 204, pp. 86-92, (2016) (PubMed).

Kiasalari, Baluchnejadmojarad, Roghani: "Hypericum Perforatum Hydroalcoholic Extract Mitigates Motor Dysfunction and is Neuroprotective in Intrastriatal 6-Hydroxydopamine Rat Model of Parkinson's Disease." dans: Cellular and molecular neurobiology, Vol. 36, Issue 4, pp. 521-30, (2016) (PubMed).

Kiasalari, Khalili, Baluchnejadmojarad, Roghani: "Protective Effect of Oral Hesperetin Against Unilateral Striatal 6-Hydroxydopamine Damage in the Rat." dans: Neurochemical research, Vol. 41, Issue 5, pp. 1065-72, (2016) (PubMed).

Tskitishvili, Pequeux, Munaut, Viellevoye, Nisolle, Noël, Foidart: "Estrogen receptors and estetrol-dependent neuroprotective actions: a pilot study." dans: The Journal of endocrinology, Vol. 232, Issue 1, pp. 85-95, (2016) (PubMed).

Zarezadeh, Baluchnejadmojarad, Kiasalari, Afshin-Majd, Roghani: "Garlic active constituent s-allyl cysteine protects against lipopolysaccharide-induced cognitive deficits in the rat: Possible involved mechanisms." dans: European journal of pharmacology, Vol. 795, pp. 13-21, (2016) (PubMed).

Ahshin-Majd, Zamani, Kiamari, Kiasalari, Baluchnejadmojarad, Roghani: "Carnosine ameliorates cognitive deficits in streptozotocin-induced diabetic rats: Possible involved mechanisms." dans: Peptides, Vol. 86, pp. 102-111, (2016) (PubMed).

Park, Shim, An, Starkweather, Kim, Shim: "IL-4 Inhibits IL-1β-Induced Depressive-Like Behavior and Central Neurotransmitter Alterations." dans: Mediators of inflammation, Vol. 2015, pp. 941413, (2015) (PubMed).

Tskitishvili, Nisolle, Munaut, Pequeux, Gerard, Noel, Foidart: "Estetrol attenuates neonatal hypoxic-ischemic brain injury." dans: Experimental neurology, Vol. 261, pp. 298-307, (2014) (PubMed).

Détail du antigène

Antigène: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Abstract: GFAP Produits

Synonymes: GFAP Kit ELISA, AI836096 Kit ELISA, cb345 Kit ELISA, etID36982.3 Kit ELISA, gfapl Kit ELISA, wu:fb34h11 Kit ELISA, wu:fk42c12 Kit ELISA, xx:af506734 Kit ELISA, zgc:110485 Kit ELISA, glial fibrillary acidic protein Kit ELISA, GFAP Kit ELISA, LOC100136168 Kit ELISA, gfap Kit ELISA, Gfap Kit ELISA

UniProt: P47819