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Rat TGF-β1 ELISA kitEK0524

  Catalog No. Package Size Price
EK0524-1 1x96T $399.00
EK0524-2 5x96T $1799.00
EK0524-3 10x96T $3459.00

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Description
  • Product Name Rat TGF-β1 ELISA kit
  • Brief Description ELISA Kit
  • Applications Solid Phase Sandwich ELISA
  • Species Reactivity Rat
  • Specificity Natural and recombinant Rat TGF-β1 Ligand
  • Crossing Reactivity No significant interference observed with available related molecules.
  • Target Name Rat TGF-β1
Application Details

Detect Range: 0.06 - 4.0 ng/mL
Sensitivity: 15pg/mL
Sample Type: Cell culture supernatant, serum, plasma (EDTA, citrate, heparin)
Sample Volume: 20 uL
Assay Time: 3 hour
Detection method: Colorimetric

Images
  • Rat TGF-β1 ELISA kit - Absci

    Representative standard curve for TGF-β1 ELISA. TGF-β1 was diluted in serial two-fold steps in Sample Diluent.

Product Description
  • Aluminium pouches with a Microwell Plate coated with antibody to rat TGF-β1 (8x12)
  • 2 vials rat TGF-β1 Standard lyophilized, 2000 pg/ml upon reconstitution
  • 2 vials concentrated Biotin-Conjugate anti-rat TGF-β1 antibody
  • 2 vials Streptavidin-HRP solution
  • 4 bottle Standard /sample Diluent
  • 1 bottle Biotin-Conjugate antibody Diluent
  • 1 bottle Streptavidin-HRP Diluent
  • 1 bottle Wash Buffer Concentrate 20x (PBS with 1% Tween-20)
  • 1 vial Substrate Solution
  • 1 vial Stop Solution
  • 2 vial 1N HCl
  • 2 vial 1.2 N NaOH/0.5M HEPES
  • 4 pieces Adhesive Films
  • package insert
Background

Transforming growth factor (TGF), a 'factor' that promoted the transformation of cultured fibroblasts into a tumor-like phenotype, was subsequently found to be more of a tumor suppressor than tumor promoter and to be a mixture of two proteins, TGF-α and TGF-β. These molecules are members of a superfamily that includes TGF-β1 through 5, bone morphogenic proteins, activins and inhibins. It plays a critical role in cellular growth, development, differentiation, proliferation, extracellular matrix (ECM) synthesis and degradation, control of mesenchymal-epithelial interactions during embryogenesis, immune modulation, apoptosis, cell cycle progression, angiogenesis, adhesion and migration and leukocyte chemotaxis.

Originally, TGF-β1 was separated from platelets and later found that TGF-β1 can be expressed in many organizations. Human TGF-β1 is a 25kDa, disulfide-linked, non-glycosylated homodimer. Biological activity of TGF-β1 is regulated by a number of receptors, including receptor I (53-65KD), receptor II (83-110KD), receptor III (250-310KD), receptor-IV (60KD) and receptor V (400KD).

TGF-β1 is the key mediator in the pathophysiology of tissue repair and human fibrogenesis: balance between production and degradation of type I collagen, and fibrosis and scarring in organ and tissue. TGF-β1 exhibits important immunoregulatory features of partially adverse character: TGF-β1 inhibits B and T cell proliferation, differentiation and antibody production as well as maturation and activation of macrophages. TGF-β1 is synthesized, with only a few exceptions, by virtually all cells, and TGF receptors are expressed by all cells. TGF-β affects nearly every physiological process in some way; its systemic and cell-specific activities are too complicated to review here. There are, however, three fundamental activities: TGF-β1 modulates cell proliferation, generally as a suppressor; TGF-β1 enhances the deposition of extracellular matrix through promotion of synthesis and inhibition of degradation; TGF-β1 is immunosuppressive through a variety of mechanisms. The specific action of TGF-β on a particular cell depends on the exact circumstances of that cell's environment.

Regerences

Kingsley, D.M. (1994) Genes Dev. 8:133.

Javelaud, D. and A. Mauviel (2004) Int. J. Biochem. Cell Biol. 36:1161.

Chang, H. et al. (2002) Endocr. Rev. 23:787.

Kondaiah, P. et al. (1988) J. Biol. Chem. 263:18313.

Clark, D.A. and R. Coker (1998) Int. J. Biochem. Cell Biol. 30:293.

Qian, S.W. et al. (1990) Nucleic Acids Res. 18:3059.

Derynack, R. et al. (1986) J. Biol. Chem. 261:4377.

Dubois, C.M. et al. (1995) J. Biol. Chem. 270:10618.

Manning, A.M. et al. (1995) Gene 155:307.

Brunner, A.M. et al. (1989) J. Biol. Chem. 264:13660.

Mittl, P.R.E. et al. (1996) Protein Sci. 5:1261.

Gray, A.M. and A.J. Mason (1990) Science 247:1328.

Oklu, R. and R. Hesketh (2000) Biochem. J. 352:601.

Saharinen, J. et al. (1996) EMBO J. 15:245.

Mangasser-Stephan, K. and A.M. Gressner (1999) Cell Tissue Res. 297:363.

Koli, K. et al. (2001) J. Cell Sci. 114:2869.

Yang, L. et al. (2000) Wound Rep. Reg. 8:538.

Pedrozo, H.A. et al. (1999) Endocrinology 140:5806.

Yu, Q. and I. Stamenkovic (2000) Genes Dev. 14:163.

Maeda, S. et al. (2001) J. Bone Miner. Res. 16:1281.

Munger, J.S. et al. (1999) Cell 96:319.

Derynck, R. et al. (1985) Nature 316:701.

Derynck, R. and X-H. Feng (1997) Biochim. Biophys. Acta 1333:F105.

Ten Dijke, P. et al. (1996) Curr. Opin. Cell. Biol. 8:139.

Chai, Y. et al. (2003) Crit. Rev. Oral Biol. Med. 14:78.

de Caestecker, M. et al. (2004) Cytokine Growth Factor Rev. 15:1.

    Please let us know if you have published research using #EK0524 so that we can cite your reference.
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    Protocol
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    Note
      Application:
    • WBWestern Blotting
    • IHCImmunohistochemistry
    • IFImmunofluorescence
    • ICCImmunocytochemistry
    • FCFlow Cytometry
    • IPImmunoprecipitation
    • EELISA
    • DBDot Blotting
    • ChIPChromatin Immunoprecipitation
    • GICAGold Immunochromatography Assay
    • NCNegative Control
      Species Reactivity:
    • HuHuman
    • MsMouse 
    • RtRat 
    • Dm Drosophila melanogaster
    • C Caenorhabditis elegans
    • MkMonkey
    • RbRabbit
    • B Bovine 
    • D Dog
    • PPig
    • HmHamster
    • ChHm Chinese Hamster 
    • ChkChicken  
    • ShpSheep  


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