Nerve Growth Factor beta (NGFB) ELISA Kit

Details for Product No. ABIN624954
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Target Name (Antigen)
Synonyms NGFB, beta-NGF, Beta-NGF, HSAN5, Ngfb, ngfb, ns:zft386, xx:zft386, zgc:109730, hsan5, beta-ngf
Reactivity
Alternatives Human
Kits with alternative reactivity to:
(3), (2), (2), (5), (3), (3), (4), (1)
Application
ELISA
Pubmed 1 reference available
Catalog no. ABIN624954
Quantity 96 tests
Price
416.90 $   Plus shipping costs $45.00
Options
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Availability Will be delivered in 5 to 7 Business Days

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Sample Type Serum, Plasma, Cell Culture Supernatant, Urine
Specificity This ELISA kit shows no cross-reactivity with the following cytokines tested: human Angiogenin, BDNF, BLC, ENA-78, FGF-4, IL-1 alpha, IL-1beta, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12 p70, IL-12 p40, IL-13, IL-15, IL-309, IP-10, G-CSF, GM-CSF, IFN- gamma, Leptin (OB), MCP-1, MCP-3, MDC, MIP-1 alpha, MIP-1 beta, MIP-1delta, MMP-1, - 2, -3, -10, PARC, RANTES, SCF, TARC, TGF- beta, TIMP-1, TIMP-2, TNF-alpha, TNF- beta, TPO, VEGF.
Sensitivity The minimum detectable dose of beta-NGF is typically less than 14 pg/ml.
Characteristics Human beta-NGF ELISA Kit For Serum, Plasma, Cell Culture Supernatant and Urine
Components 1. Beta-NGF Microplate (Item A): 96 wells (12 strips x 8 wells) coated with anti-human beta-NGF. 2. Wash Buffer Concentrate (20x) (Item B): 25 ml of 20x concentrated solution. 3. Standards (Item C): 2 vials, recombinant human beta-NGF. 4. Assay Diluent (Item E): 15 ml of 5x concentrated buffer. For Standard/Sample (serum/plasma samples/cell culture medium/urine) diluent. 5. Detection Antibody beta-NGF (Item F): 2 vial of biotinylated anti- human beta-NGF (each vial is enough to assay half microplate). 6. HRP-Streptavidin concentrate (Item G): 8 µl 40,000x concentrated HRP-conjugated streptavidin. 7. TMB One-Step Substrate Reagent (Item H): 12 ml of 3,3™,5,5™- tetramethylbenzidine (TMB) in buffered solution. 8. Stop Solution (Item I): 8 ml of 2 M sulfuric acid.
Material not included 1. Microplate reader capable of measuring absorbance at 450 nm. 2. Precision pipettes to deliver 2 µl to 1 ml volumes. 3. Adjustable 1-25 ml pipettes for reagent preparation. 4. 100 ml and 1 liter graduated cylinders. 5. Absorbent paper. 6. Distilled or deionized water. 7. Log-log graph paper or computer and software for ELISA data analysis. 8. Tubes to prepare standard or sample dilutions.
Alternative Name beta-NGF
Background The Human beta-NGF (beta-nerve growth factor) ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of human beta-NGF in serum, plasma, cell culture supernatants and urine. This assay employs an antibody specific for human beta-NGF coated on a 96-well plate. Standards and samples are pipetted into the wells and beta-NGF present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-human beta-NGF antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of beta-NGF bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm. Reproducibility: Intra-Assay: CV<10% Inter-Assay: CV<12%.
Plate 96 wells
Reagent Preparation 1. Bring all reagents and samples to room temperature (18 - 25°C) before use. 2. Sample dilution: If your samples need to be diluted, Assay Diluent (Item E) is used for dilution of serum/plasma/culture supernatants/urine. 3. Assay Diluent (Item E) should be diluted 5-fold with deionized or distilled water before use. 4. Preparation of standard: Briefly spin the vial of Item C. Add 400 µl 1x Assay Diluent (Item E) into Item C vial to prepare a 50 ng/ml standard solution. Dissolve the powder thoroughly by a gentle mix. Add 50 µl beta-NGF standard from the vial of tem C, into a tube with 450 µl 1x Assay Diluent to prepare a 5,000 pg/ml standard solution. Pipette 400 µl 1x Assay Diluent into each tube. Use the 5,000 pg/ml standard solution to produce a dilution series (shown below). Mix each tube thoroughly before the next transfer. Gently vortex to mix. 1x Assay Diluent serves as the zero standard (0 pg/ml). 5. If the Wash Concentrate (20x) (Item B) contains visible crystals, warm to room temperature and mix gently until dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to yield 400 ml of 1x Wash Buffer. 6. Briefly spin the Detection Antibody vial (Item F) before use. Add 100 µl of 1x Assay Diluent into the vial to prepare a detection antibody concentrate. Pipette up and down to mix gently (the concentrate can be stored at 4°C for 5 days). The detection antibody concentrate should be diluted 80-fold with 1x Assay Diluent and used in step 4 of Part VI Assay Procedure. 7. Briefly spin the HRP-Streptavidin concentrate vial (Item G) and pipette up and down to mix gently before use. HRP-Streptavidin concentrate should be diluted 40,000-fold with 1x Assay Diluent. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 2 µl of HRP-Streptavidin concentrate into a tube with 198.0 µl 1x Assay Diluent to prepare a 100-fold diluted HRP-Streptavidin solution (do not store the diluted solution for next day use). Mix through and then pipette 30 µl of prepared 100-fold diluted solution into a tube with 12 ml 1x Assay Diluent to prepare a final 40,000 fold diluted HRP-Streptavidin solution.
Assay Procedure 1. Bring all reagents and samples to room temperature (18 - 25°C) before use. It is recommended that all standards and samples be run at least in duplicate. 2. Add 100 µl of each standard (see Reagent Preparation step 2) and sample into appropriate wells. Cover well and incubate for 2.5 hours at room temperature or over night at 4°C with gentle shaking. 3. Discard the solution and wash 4 times with 1x Wash Solution. Wash by filling each well with Wash Buffer (300 µl) using a multi-channel Pipette or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels. 4. Add 100 µl of 1x prepared biotinylated antibody (Reagent Preparation step 6) to each well. Incubate for 1 hour at room temperature with gentle shaking. 5. Discard the solution. Repeat the wash as in step 3. 6. Add 100 µl of prepared Streptavidin solution (see Reagent Preparation step 7) to each well. Incubate for 45 minutes at room temperature with gentle shaking. 7. Discard the solution. Repeat the wash as in step 3. 8. Add 100 µl of TMB One-Step Substrate Reagent (Item H) to each well. Incubate for 30 minutes at room temperature in the dark with gentle shaking. 9. Add 50 µl of Stop Solution (Item I) to each well. Read at 450 nm immediately.
Calculation of Results Calculate the mean absorbance for each set of duplicate standards, controls and samples, and subtract the average zero standard optical density. Plot the standard curve on log-log graph paper or using Sigma plot software, with standard concentration on the x-axis and absorbance on the y-axis. Draw the best-fit straight line through the standard points.
Restrictions For Research Use only
Storage 4 °C
Product cited in: Kalinowska-Łyszczarz, Pawlak, Michalak et al.: "Immune cell NT-3 expression is associated with brain atrophy in multiple sclerosis patients." in: Journal of neuroimmunology, 2011 (PubMed).

Reactivities (3), (2), (2), (5), (3), (3), (4), (1)
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