Human IGFBP-3 DuoSet ELISA

Catalog # Availability Size / Price Qty
DY675
Ancillary Products Available

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Human IGFBP-3 ELISA Standard Curve
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Product Details
Procedure
Citations (13)
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Reviews (3)

Human IGFBP-3 DuoSet ELISA Summary

Assay Type
Solid Phase Sandwich ELISA
Format
96-well strip plate
Sample Volume Required
100 µL
Assay Range
125.0 - 8,000 pg/mL
Sufficient Materials
For fifteen 96-well plates*
Specificity
Please see the product datasheet

* Provided that the recommended microplates, buffers, diluents, substrates and solutions are used, and the assay is run as summarized in the Assay Procedure provided.

This DuoSet ELISA Development kit contains the basic components required for the development of sandwich ELISAs to measure natural and recombinant human IGFBP-3. The suggested diluent is suitable for the analysis of most cell culture supernate samples. Diluents for complex matrices, such as serum and plasma, should be evaluated prior to use in this DuoSet.

Product Features

  • Optimized capture and detection antibody pairings with recommended concentrations save lengthy development time
  • Development protocols are provided to guide further assay optimization
  • Assay can be customized to your specific needs
  • Economical alternative to complete kits

Kit Content

  • Capture Antibody
  • Detection Antibody
  • Recombinant Standard
  • Streptavidin conjugated to horseradish-peroxidase (Streptavidin-HRP)

Other Reagents Required

DuoSet Ancillary Reagent Kit 3 (5 plates): (Catalog # DY009) containing 96 well microplates, plate sealers, substrate solution, stop solution, plate coating buffer (PBS), wash buffer, and Reagent Diluent Concentrate 3.

Normal Goat Serum: (Catalog # DY005)

 

The components listed above may be purchased separately:

PBS: (Catalog # DY006), or 137 mM NaCl, 2.7 mM KCl, 8.1 mM Na2HPO4, 1.5 mM KH2PO4, pH 7.2 - 7.4, 0.2 µm filtered

Wash Buffer: (Catalog # WA126), or 0.05% Tween® 20 in PBS, pH 7.2-7.4

Reagent Diluent: 5% Tween 20 plus 2% Normal Goat Serum in PBS
pH 7.2-7.4, 0.2 μm filtered (R&D Systems®, Catalog # DY004 and
DY005).

Substrate Solution: 1:1 mixture of Color Reagent A (H2O2) and Color Reagent B (Tetramethylbenzidine) (Catalog # DY999)

Stop Solution: 2 N H2SO4 (Catalog # DY994)

Microplates: R&D Systems (Catalog # DY990)

Plate Sealers: ELISA Plate Sealers (Catalog # DY992)

 

Scientific Data

Human IGFBP-3 ELISA Standard Curve

Product Datasheets

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Preparation and Storage

Shipping
The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store the unopened product at 2 - 8 °C. Do not use past expiration date.

Background: IGFBP-3

The superfamily of insulin-like growth factor (IGF) binding proteins include the six high-affinity IGF binding proteins (IGFBP) and at least four additional low-affinity binding proteins referred to as IGFBP related proteins (IGFBP-rP). All IGFBP superfamily members are cysteine-rich proteins with conserved cysteine residues, which are clustered in the amino- and carboxy-terminal thirds of the molecule. IGFBPs modulate the biological activities of IGF proteins. Some IGFBPs may also have intrinsic bioactivity that is independent of their ability to bind IGF proteins. Post-translational modifications of IGFBP, including glycosylation, phosphorylation and proteolysis, have been shown to modify the affinities of the binding proteins to IGF. ALS (Acid Labile Subunit) is a liver-derived protein that exists in a ternary complex with Insulin-like Growth Factor (IGF)-binding Protein-3 (IGFBP-3) or IGFBP-5, and either IGF-I or IGF-II. ALS increases the half-life of IGF/IGFBP complexes in circulation.

Long Name:
Insulin-like Growth Factor Binding Protein 3
Entrez Gene IDs:
3486 (Human); 16009 (Mouse)
Alternate Names:
acid stable subunit of the 140 K IGF complex; binding protein 29; binding protein 53; growth hormone-dependent binding protein; IBP-3; IBP3BP-53; IGF-binding protein 3; IGFBP3; IGFBP-3; insulin-like growth factor binding protein 3; insulin-like growth factor-binding protein 3

Assay Procedure

GENERAL ELISA PROTOCOL


Plate Preparation

  1. Dilute the Capture Antibody to the working concentration in PBS without carrier protein. Immediately coat a 96-well microplate with 100 μL per well of the diluted Capture Antibody. Seal the plate and incubate overnight at room temperature.
  2. Aspirate each well and wash with Wash Buffer, repeating the process two times for a total of three washes. Wash by filling each well with Wash Buffer (400 μL) using a squirt bottle, manifold dispenser, or autowasher. Complete removal of liquid at each step is essential for good performance. After the last wash, remove any remaining Wash Buffer by aspirating or by inverting the plate and blotting it against clean paper towels.
  3. Block plates by adding 300 μL of Reagent Diluent to each well. Incubate at room temperature for a minimum of 1 hour.
  4. Repeat the aspiration/wash as in step 2. The plates are now ready for sample addition.

Assay Procedure

  1. Add 100 μL of sample or standards in Reagent Diluent, or an appropriate diluent, per well. Cover with an adhesive strip and incubate 2 hours at room temperature.
  2. Repeat the aspiration/wash as in step 2 of Plate Preparation.
  3. Add 100 μL of the Detection Antibody, diluted in Reagent Diluent, to each well. Cover with a new adhesive strip and incubate 2 hours at room temperature.
  4. Repeat the aspiration/wash as in step 2 of Plate Preparation.
  5. Add 100 μL of the working dilution of Streptavidin-HRP to each well. Cover the plate and incubate for 20 minutes at room temperature. Avoid placing the plate in direct light.
  6. Repeat the aspiration/wash as in step 2.
  7. Add 100 μL of Substrate Solution to each well. Incubate for 20 minutes at room temperature. Avoid placing the plate in direct light.
  8. Add 50 μL of Stop Solution to each well. Gently tap the plate to ensure thorough mixing.
  9. Determine the optical density of each well immediately, using a microplate reader set to 450 nm. If wavelength correction is available, set to 540 nm or 570 nm. If wavelength correction is not available, subtract readings at 540 nm or 570 nm from the readings at 450 nm. This subtraction will correct for optical imperfections in the plate. Readings made directly at 450 nm without correction may be higher and less accurate.

Citations for Human IGFBP-3 DuoSet ELISA

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

13 Citations: Showing 1 - 10
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  1. Prediction of emergency cerclage outcomes in women with cervical insufficiency: The role of inflammatory, angiogenic, and extracellular matrix-related proteins in amniotic fluid
    Authors: KN Lee, KH Park, YM Kim, I Cho, TE Kim
    PLoS ONE, 2022-05-10;17(5):e0268291.
    Species: Human
    Sample Types: Amniotic Fluid
  2. Dipeptidyl peptidase-4 inhibitors reduced long-term cardiovascular risk in diabetic patients after percutaneous coronary intervention via insulin-like growth factor-1 axis
    Authors: Y Chikata, H Iwata, K Miyosawa, T Koike, H Yasuda, T Funamizu, S Doi, H Endo, H Wada, R Naito, M Ogita, T Dohi, T Kasai, K Isoda, S Okazaki, K Miyauchi, T Minamino
    Scientific Reports, 2022-03-24;12(1):5129.
    Species: Human
    Sample Types: Serum
  3. A standardized gnotobiotic mouse model harboring a minimal 15-member mouse gut microbiota recapitulates SOPF/SPF phenotypes
    Authors: M Darnaud, F De Vadder, P Bogeat, L Boucinha, AL Bulteau, A Bunescu, C Couturier, A Delgado, H Dugua, C Elie, A Mathieu, T Novotná, DA Ouattara, S Planel, A Saliou, D Šr?tková, J Yansouni, B Stecher, M Schwarzer, F Leulier, A Tamellini
    Nature Communications, 2021-11-18;12(1):6686.
    Species: Mouse
    Sample Types: Serum
  4. Effect of anthelmintic treatment on serum free IGF-1 and IGFBP-3: a cluster-randomized-controlled trial in Indonesia
    Authors: F Kurniawan, DL Tahapary, K de Ruiter, E Yunir, NR Biermasz, JWA Smit, T Supali, E Sartono, M Yazdanbakh, P Soewondo
    Sci Rep, 2020-11-04;10(1):19023.
    Species: Human
    Sample Types: Serum
  5. Using a cultural dance program to increase sustainable physical activity for breast cancer survivors-A pilot study
    Authors: LWM Loo, K Nishibun, L Welsh, T Makolo, CD Chong, I Pagano, H Yu, EO Bantum
    Complement Ther Med, 2019-09-21;47(0):102197.
    Species: Human
    Sample Types: Plasma
  6. MODELING STROMA-INDUCED DRUG RESISTANCE IN A TISSUE-ENGINEERED TUMOR MODEL OF EWING SARCOMA
    Authors: Marco Santoro
    Tissue Eng Part A, 2017-01-01;0(0):.
    Species: Human
    Sample Types: Cell Culture Supernates
  7. Antitumor activity and immunogenicity of recombinant vaccinia virus expressing HPV 16 E7 protein SigE7LAMP is enhanced by high-level coexpression of IGFBP-3.
    Authors: Musil, J, Kutinova, L, Zurkova, K, Hainz, P, Babiarova, K, Krystofova, J, Nemeckova, S
    Cancer Gene Ther, 2014-02-21;21(3):115-25.
    Species: Mouse, Primate - Chlorocebus aethiops (African Green Monkey)
    Sample Types: Cell Lysates
  8. Human IGF Binding Protein-3 Overexpression Impairs Glucose Regulation in Mice via an Inhibition of Insulin Secretion.
    Authors: Nguyen KH, Yao XH, Moulik S, Mishra S, Nyomba BL
    Endocrinology, 2011-03-29;152(6):2184-96.
    Species: Human
    Sample Types: Plasma
  9. Biological effects induced by insulin-like growth factor binding protein 3 (IGFBP-3) in malignant melanoma.
    Authors: Oy GF, Slipicevic A, Davidson B, Solberg Faye R, Maelandsmo GM, Florenes VA
    Int. J. Cancer, 2010-01-15;126(2):350-61.
    Species: Human
    Sample Types: Cell Culture Supernates
  10. IGF-I and IGFBP-3 augment transforming growth factor-beta actions in human renal carcinoma cells.
    Authors: Rosendahl AH, Forsberg G
    Kidney Int., 2006-09-13;70(9):1584-90.
    Species: Human
    Sample Types: Cell Culture Supernates
  11. Mining the acute respiratory distress syndrome proteome: identification of the insulin-like growth factor (IGF)/IGF-binding protein-3 pathway in acute lung injury.
    Authors: Schnapp LM, Donohoe S, Chen J, Sunde DA, Kelly PM, Ruzinski J, Martin T, Goodlett DR
    Am. J. Pathol., 2006-07-01;169(1):86-95.
    Species: Human
    Sample Types: BALF
  12. Thrombospondin 1, produced by endothelial cells under the action of erythropoietin, stimulates thymidine incorporation into erythroid cells and counteracts the inhibitory action of insulin-like growth factor binding protein 3.
    Authors: Congote LF, DiFalco MR, Gibbs BF
    Cytokine, 2005-03-23;30(5):248-53.
    Species: Human
    Sample Types: Whole Cells
  13. Epidermal growth factor receptor regulates aberrant expression of insulin-like growth factor-binding protein 3.
    Authors: Takaoka M, Harada H, Andl CD, Oyama K, Naomoto Y, Dempsey KL, Klein-Szanto AJ, El-Deiry WS, Grimberg A, Nakagawa H
    Cancer Res., 2004-11-01;64(21):7711-23.
    Species: Human
    Sample Types: Cell Culture Supernates

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Reviews for Human IGFBP-3 DuoSet ELISA

Average Rating: 4.3 (Based on 3 Reviews)

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Human IGFBP-3 DuoSet ELISA
By Anonymous on 09/13/2019
Sample Tested: Human serum

I used this kit for quantifying IGFBP3 in human serum and plasma and it worked well. I have used 2X 15 plates so far.


Human IGFBP-3 DuoSet ELISA
By Carmen Martin-Ruiz on 08/15/2019
Sample Tested: Heparin Plasma

Used on EDTA Plasma at 1/200 dilution in RD buffer with 550nm correction and 4PL regression fitting. Very confident with the results.


Human IGFBP-3 DuoSet ELISA
By Jonatan Dereke on 08/06/2019
Sample Tested: EDTA Plasma

The booklet states that Ancillary kit 3 (DY009) can be used to run this analysis. It also states that you can buy the parts separately and that Normal Goat Serum is required for the analysis, something that ís not included in Ancillary kit 3. This detail is well hidden and led to several runs being wasted before this detail was found in the booklet, When Normal Goat Serum was added, the analysis ran satisfactorily, We ran human EDTA-plasma at a 1:400 dilution for this analysis.