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TGFB1 ELISA Kit

This Human TGFB1 ELISA Kit is a Colorimetric ELISA Kit designed to quantify Human TGFB1. This ELISA Kit has been cited in 8+ publications.
Catalog No. ABIN1889382

Quick Overview for TGFB1 ELISA Kit (ABIN1889382)

Target

See all TGFB1 ELISA Kits
TGFB1 (Transforming Growth Factor, beta 1 (TGFB1))

Binding Specificity

AA 30-278

Reactivity

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Human

Detection Method

Colorimetric

Method Type

Sandwich ELISA

Detection Range

62.5-4000 pg/mL

Application

ELISA

Sample Type

Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA)
  • Minimum Detection Limit

    62.5 pg/mL

    Purpose

    Sandwich High Sensitivity ELISA kit for Quantitative Detection of Human LAP(TGF-beta1)

    Brand

    PicoKine™

    Analytical Method

    Quantitative

    Specificity

    Expression system for standard: sf21
    Immunogen sequence: L30-R278

    Cross-Reactivity (Details)

    There is no detectable cross-reactivity with other relevant proteins.

    Sensitivity

    <10pg/mL

    Material not included

    Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl

    Immunogen

    Expression system for standard: sf21
    Immunogen sequence: L30-R278
  • Application Notes

    Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.

    Comment

    Sequence similarities: Belongs to the TGF-beta family.

    Tissue Specificity: Highly expressed in bone. Abundantly expressed in articular cartilage and chondrocytes and is increased in osteoarthritis (OA). Colocalizes with ASPN in chondrocytes within OA lesions of articular cartilage. .

    Plate

    Pre-coated

    Protocol

    human LAP(TGF-beta1) ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for LAP(TGF-beta1) has been precoated onto 96-well plates. Standards(sf21, L30-R278) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for LAP(TGF-beta1) is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the human LAP(TGF-beta1) amount of sample captured in plate.

    Assay Procedure

    Aliquot 0.1 mL per well of the 4000pg/mL, 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL human LAP(TGF-beta1) standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of human cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each human LAP(TGF-beta1) standard solution and each sample be measured in duplicate.

    Assay Precision

    • Sample 1: n=16, Mean(pg/ml): 347, Standard deviation: 13.88, CV(%): 4
    • Sample 2: n=16, Mean(pg/ml): 1638, Standard deviation: 85.18, CV(%): 5.2
    • Sample 3: n=16, Mean(pg/ml): 2586, Standard deviation: 163, CV(%): 6.3,
    • Sample 1: n=24, Mean(pg/ml): 511, Standard deviation: 29.64, CV(%): 5.8
    • Sample 2: n=24, Mean(pg/ml): 1825, Standard deviation: 100.4, CV(%): 5.5
    • Sample 3: n=24, Mean(pg/ml): 3120, Standard deviation: 246.5, CV(%): 7.9

    Restrictions

    For Research Use only
  • Handling Advice

    Avoid multiple freeze-thaw cycles.

    Storage

    -20 °C,4 °C

    Storage Comment

    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles

    Expiry Date

    12 months
  • Gong, Wang, Yuan, Li, Gu, Zhao, Zhang, Jia, Feng, Liu: "Inhibition of Tumor Growth and Immunomodulatory Effects of Flavonoids and Scutebarbatines of Scutellaria barbata D. Don in Lewis-Bearing C57BL/6 Mice." in: Evidence-based complementary and alternative medicine : eCAM, Vol. 2015, pp. 630760, (2015) (PubMed).

    Sharifi, Amani, Hajiani, Cheraghian: "Does vitamin D improve liver enzymes, oxidative stress, and inflammatory biomarkers in adults with non-alcoholic fatty liver disease? A randomized clinical trial." in: Endocrine, Vol. 47, Issue 1, pp. 70-80, (2014) (PubMed).

    Chen, Qi, Feng, Wang, Bao, Wang, Xiang, Xie: "Neuroprotective effect of allicin against traumatic brain injury via Akt/endothelial nitric oxide synthase pathway-mediated anti-inflammatory and anti-oxidative activities." in: Neurochemistry international, Vol. 68, pp. 28-37, (2014) (PubMed).

    Li, Kong, Zhang, Yang: "Long-term intake of sesamin improves left ventricular remodelling in spontaneously hypertensive rats." in: Food & function, Vol. 4, Issue 3, pp. 453-60, (2013) (PubMed).

    Li, Yang, Ma, Li, Tu, Gao et al.: "Fabrication of poly(lactide-co-glycolide) scaffold filled with fibrin gel, mesenchymal stem cells, and poly(ethylene oxide)-b-poly(L-lysine)/TGF-?1 plasmid DNA complexes for cartilage restoration in ..." in: Journal of biomedical materials research. Part A, Vol. 101, Issue 11, pp. 3097-108, (2013) (PubMed).

    Gao, Huang, Li: "NOX1 abet mesangial fibrogenesis via iNOS induction in diabetes." in: Molecular and cellular biochemistry, Vol. 382, Issue 1-2, pp. 185-91, (2013) (PubMed).

    Wang, Deng, Ren, Xiao, Chen, Tao: "Lactoferrin administration into the nostril alleviates murine allergic rhinitis and its mechanisms." in: Scandinavian journal of immunology, Vol. 78, Issue 6, pp. 507-15, (2013) (PubMed).

    Shen, Zhao: "Pulsed electromagnetic fields stimulation affects BMD and local factor production of rats with disuse osteoporosis." in: Bioelectromagnetics, Vol. 31, Issue 2, pp. 113-9, (2010) (PubMed).

  • Target See all TGFB1 ELISA Kits

    TGFB1 (Transforming Growth Factor, beta 1 (TGFB1))

    Alternative Name

    TGFB1

    Background

    Protein Function: Multifunctional protein that controls proliferation, differentiation and other functions in many cell types. Many cells synthesize TGFB1 and have specific receptors for it. It positively and negatively regulates many other growth factors. It plays an important role in bone remodeling as it is a potent stimulator of osteoblastic bone formation, causing chemotaxis, proliferation and differentiation in committed osteoblasts. Can promote either T- helper 17 cells (Th17) or regulatory T-cells (Treg) lineage differentiation in a concentration-dependent manner. At high concentrations, leads to FOXP3-mediated suppression of RORC and down-regulation of IL-17 expression, favoring Treg cell development. At low concentrations in concert with IL-6 and IL-21, leads to expression of the IL-17 and IL-23 receptors, favoring differentiation to Th17 cells. .

    Background: TGFbeta1 is secreted as a latent form, which consists of its mature form and a latency-associated peptide(beta1-LAP) in either the presence or the absence of additional latent TGF-beta1-binding protein. Processing and cleavage of the precursor protein between amino acids 278 and 279 results in the formation of LAP dimers and TGF beta dimers that then non-covalently associate with each other to form the small latent TGF beta complex. LAP is secreted and can be found in the extracellular matrix. In addition, LAP can also be expressed on platelets and activated regulatory T cells.

    Synonyms: Transforming growth factor beta-1,TGF-beta-1,Latency-associated peptide,LAP,TGFB1,TGFB,

    Full Gene Name: Transforming growth factor beta-1

    Cellular Localisation: Secreted, extracellular space, extracellular matrix.

    Gene ID

    7939

    UniProt

    P01137

    Pathways

    EGFR Signaling Pathway, Dopaminergic Neurogenesis, Cellular Response to Molecule of Bacterial Origin, Glycosaminoglycan Metabolic Process, Regulation of Leukocyte Mediated Immunity, Regulation of Muscle Cell Differentiation, Positive Regulation of Immune Effector Process, Cell-Cell Junction Organization, Production of Molecular Mediator of Immune Response, Ribonucleoside Biosynthetic Process, Skeletal Muscle Fiber Development, Regulation of Carbohydrate Metabolic Process, Protein targeting to Nucleus, Autophagy, Cancer Immune Checkpoints
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