IGF1 ELISA 试剂盒 (Insulin-Like Growth Factor 1)

Details for Product IGF1 ELISA Kit No. ABIN1979604, 供应商: Log in to see
  • IGF-I
  • IGF1A
  • IGFI
  • C730016P09Rik
  • Igf-1
  • Igf-I
  • Npt2B
  • IGF-1
  • IGF-IB
  • igf1
  • IGF-1L
  • IGF-1a
  • IGF1
  • igf-1
  • igf1-A
  • igf1.S
  • xigf1
  • insulin like growth factor 1
  • insulin-like growth factor 1
  • insulin-like growth factor I
  • insulin like growth factor 1 L homeolog
  • IGF1
  • Igf1
  • LOC100136741
  • igf1
  • LOC678666
  • igf1.L

Kits with alternative reactivity to:
Sandwich ELISA
0.1-30 ng/mL
0.1 ng/mL
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原理 Human IGF-1 ELISA Kit for cell culture supernatants, plasma, and serum samples.
样品类型 Plasma, Cell Culture Supernatant, Serum
Analytical Method Quantitative
检测方法 Colorimetric
特异性 This IGF-1 ELISA kit shows no cross-reactivity with any of the cytokines tested: Human Angiogenin, BDNF, BLC, ENA-78, FGF-4, IGFBP-1, IGFBP-2, IGFBP-3, IGFBP-4, IL-1 alpha, IL-1 beta, 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, I-309, IP-10, G-CSF, GM-CSF, IFN-gamma, Leptin (OB), MCP-1, MCP-3, MDC, MIP-1 alpha, MIP-1 beta, MIP-1 delta, PARC, RANTES, SCF, TARC, TGF-beta, TIMP-1, TIMP-2, TNF-alpha, TNF-beta, TPO, VEGF.
灵敏度 100 pg/mL
  • Strip plates and additional reagents allow for use in multiple experiments
  • Quantitative protein detection
  • Establishes normal range
  • The best products for confirmation of antibody array data
  • Pre-Coated 96-well Strip Microplate
  • Wash Buffer
  • Stop Solution
  • Assay Diluent(s)
  • Lyophilized Standard
  • Biotinylated Detection Antibody
  • Streptavidin-Conjugated HRP
  • TMB One-Step Substrate
  • Distilled or deionized water
  • Precision pipettes to deliver 2 μL to 1 μL volumes
  • Adjustable 1-25 μL pipettes for reagent preparation
  • 100 μL and 1 liter graduated cylinders
  • Tubes to prepare standard and sample dilutions
  • Absorbent paper
  • Microplate reader capable of measuring absorbance at 450nm
  • Log-log graph paper or computer and software for ELISA data analysis
Plasmids, Primers & others Plasmids, Primers & others IGF1 products on genomics-online (e.g. as negative or positive controls)
别名 IGF-I (IGF1 ELISA Kit 摘要)
背景 The Human IGF-I ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of human IGF-I in serum, plasma, cell culture supernatants and urine. This assay employs an antibody specific for human IGF-I coated on a 96-well plate. Standards and samples are pipetted into the wells and IGF-I present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-human IGF-I 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 IGF-I 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%.
基因ID 3479
UniProt P05019
途径 RTK signaling, Intracellular Steroid Hormone Receptor Signaling Pathway, Peptide Hormone Metabolism, Hormone Activity, Regulation of Intracellular Steroid Hormone Receptor Signaling, Regulation of Hormone Metabolic Process, Regulation of Hormone Biosynthetic Process, Stem Cell Maintenance, Glycosaminoglycan Metabolic Process, Regulation of Carbohydrate Metabolic Process, Autophagy, Smooth Muscle Cell Migration, Activated T Cell Proliferation, Positive Regulation of fat Cell Differentiation
应用备注 Recommended Dilution for serum and plasma samples2 - 20 fold
样本量 100 μL
板类型 Pre-coated
  1. Prepare all reagents, samples and standards as instructed in the manual.
  2. Add 100 μL of standard or sample to each well.
  3. Incubate 2.5 h at RT or O/N at 4 °C.
  4. Add 100 μL of prepared biotin antibody to each well.
  5. Incubate 1 h at RT.
  6. Add 100 μL of prepared Streptavidin solution to each well.
  7. Incubate 45 min at RT.
  8. Add 100 μL of TMB One-Step Substrate Reagent to each well.
  9. Incubate 30 min at RT.
  10. Add 50 μL of Stop Solution to each well.
  11. Read at 450 nm immediately.
  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 C (Item L) should be used for dilution of serum/plasma/culture supernatants/urine. Suggested dilution for normal serum/plasma: 2-20 fold. Please note that levels of the target protein may vary between different specimens. Optimal dilution factors for each sample must be determined by the investigator.
    3. Preparation of standard: Briefly spin the vial of Item C and then add 400 µL Assay Diluent C into Item C vial to prepare a 100 ng/mL standard. Dissolve the powder thoroughly by a gentle mix. Add 150 µL IGF-I standard from the vial of Item C, into a tube with 350 µL Assay Diluent C to prepare a 30 ng/mL standard solution. Pipette 300 µL Assay Diluent C into each tube. Use the 30 ng/mL standard solution to produce a dilution series . Mix each tube thoroughly before the next transfer. Assay Diluent C serves as the zero standard (0 ng/mL). 200 µL 200myl 200 µL 200 µL 200 µL 200 µL 150 µL Standard + 350 µL 30 12 4.8 1.92 0.768 0.307 0.123 0 ng/mL ng/mL ng/mL ng/mL ng/mL ng/mL ng/mL ng/mL
    4. 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.
    5. Briefly spin the Detection Antibody vial (Item F) before use. Add 100 µL of Assay Diluent C 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 Assay Diluent C and used in step 4 of Part VI Assay Procedure.
    6. Briefly spin the HRP-Streptavidin concentrate vial (Item G) before use. HRP-Streptavidin concentrate should be diluted 120-fold with Assay Diluent C. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 100 µL of HRP-Streptavidin concentrate into a tube with 12 ml Assay Diluent C to prepare a final 120 fold diluted HRP- Streptavidin solution (don't store the diluted solution for next day use). Mix well.
  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 myl) 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 5) to each well. Incubate for 1 hour at room temperature with gentle shaking.
    5. Discard the solution. Repeat the wash as in step
    6. Add 100 µL of prepared Streptavidin solution (see Reagent Preparation step 6) to each well. Incubate for 45 minutes at room temperature with gentle shaking.
    7. Discard the solution. Repeat the wash as in step
    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.

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.
Typical Data: These standard curves are for demonstration only. A standard curve must be run with each assay. Assay Diluent C Human IGF-I concentration (ng/mL) O D =4 50 n m 0.01 0.1 1 10 0.01 0.1 1 10 100
Sensitivity: The minimum detectable dose of IGF-1 is typically less than 0.1 ng/mL.
Recovery: Recovery was determined by spiking various levels of IGF-1 into human serum, plasma and cell culture media. Mean recoveries are as follows: Sample Type Average % Recovery Range ( %) Serum 119.6 105-138 Plasma 105.4 81-121 Cell culture media 102.5 98-110
Linearity: Sample Type Serum Plasma Cell Culture Media 1:2 Average % of Expected 116.4 111.9 103.3 Range ( %) 108-124 107-125 94-118 1:4 Average % of Expected 121.9 104.6 84.62 Range ( %) 114-130 81-120 77-92
Reproducibility: Intra-Assay: CV<10 % Inter-Assay: CV<12 %

实验精密度 Intra-Assay: CV< 10 % Inter-Assay: CV< 12 %
限制 仅限研究用
注意事项 Avoid repeated freeze-thaw cycles.
储存条件 -20 °C
储存方法 The entire kit may be stored at -20°C for up to 1 year from the date of shipment. Avoid repeated freeze-thaw cycles. The kit may be stored at 4°C for up to 6 months. For extended storage, it is recommended to store at -80°C.
有效期 6 months
ELISA image for Insulin-Like Growth Factor 1 (IGF1) ELISA Kit (ABIN1979604) Insulin-Like Growth Factor 1 (IGF1) ELISA Kit
有引用在: Shen, Lie, Miao, Yu, Lu, Feng, Li, Zu, Liu, Li: "Conditioned medium from umbilical cord mesenchymal stem cells induces migration and angiogenesis." in: Molecular medicine reports, Vol. 12, Issue 1, pp. 20-30, 2015 (PubMed).

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Ritsche, Nindl, Wideman: "Exercise-Induced growth hormone during acute sleep deprivation." in: Physiological reports, Vol. 2, Issue 10, 2014 (PubMed).

Krogh, Rostrup, Thomsen, Elfving, Videbech, Nordentoft: "The effect of exercise on hippocampal volume and neurotrophines in patients with major depression--a randomized clinical trial." in: Journal of affective disorders, Vol. 165, pp. 24-30, 2014 (PubMed).

Aucouturier, Thivel, Isacco, Fellmann, Chardigny, Duclos, Duché: "Combined food intake and exercise unmask different hormonal responses in lean and obese children." in: Applied physiology, nutrition, and metabolism = Physiologie appliquée, nutrition et métabolisme, Vol. 38, Issue 6, pp. 638-43, 2013

Aucouturier, Thivel, Isacco, Fellmann, Chardigny, Duclos, Duché: "Combined food intake and exercise unmask different hormonal responses in lean and obese children." in: Applied physiology, nutrition, and metabolism = Physiologie appliquée, nutrition et métabolisme, Vol. 38, Issue 6, pp. 638-43, 2013 (PubMed).

De Barros, Dehez, Arnaud, Barreau, Cazavet, Perez, Galinier, Casteilla, Planat-Bénard: "Aging-related decrease of human ASC angiogenic potential is reversed by hypoxia preconditioning through ROS production." in: Molecular therapy : the journal of the American Society of Gene Therapy, Vol. 21, Issue 2, pp. 399-408, 2013 (PubMed).

Kim, Kang, Krueger, Sen, Holcomb, Chen, Wenke, Yang: "Sequential delivery of BMP-2 and IGF-1 using a chitosan gel with gelatin microspheres enhances early osteoblastic differentiation." in: Acta biomaterialia, Vol. 8, Issue 5, pp. 1768-77, 2012 (PubMed).

Nwozo, Oyinloye: "Hepatoprotective effect of aqueous extract of Aframomum melegueta on ethanol-induced toxicity in rats." in: Acta biochimica Polonica, Vol. 58, Issue 3, pp. 355-8, 2012 (PubMed). (Sample species: Human). Further details: Sample: Conditioned Media (DU145 (HTB-81) cells)

Shen, Hu, Lo, Chen, Sun, Lin, Chen: "Comparison of corneal epitheliotrophic capacity among different human blood-derived preparations." in: Cornea, Vol. 30, Issue 2, pp. 208-14, 2011 (PubMed). (Sample species: Human). Further details: Sample: Plasma

Montero, Shields, Bianciotto, Shields, Ehya: "Iris metastasis from adenoid cystic carcinoma of parotid gland." in: Cornea, Vol. 30, Issue 3, pp. 351-3, 2011 (PubMed). (Sample species: Human). Further details: Sample: Cord blood serum

Bradley: "Cautery fixation for amniotic membrane transplant in pterygium surgery." in: Cornea, Vol. 30, Issue 2, pp. 194-5, 2011 (PubMed). (Sample species: Human). Further details: Sample: Serum

Guillén, Megías, Gomar, Alcaraz: "Haem oxygenase-1 regulates catabolic and anabolic processes in osteoarthritic chondrocytes." in: The Journal of pathology, Vol. 214, Issue 4, pp. 515-22, 2008 (PubMed).