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Recombinant Human Noggin Protein 25 UG

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Recombinant Human Noggin Protein 25 UG信息二維碼

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產(chǎn)品介紹

    基本參數(shù)

    詳細說明

    • Purity

      >95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie? Blue Staining.

    • Endotoxin Level

      <0.10 EU per 1 μg of the protein by the LAL method.  

    • Activity

      Measured by its ability to inhibit BMP-4-induced alkaline phosphatase production by ATDC5 mouse chondrogenic cells. The ED    50 for this effect is 0.04?0.2 μg/mL in the presence of 50 ng/mL of Recombinant Human BMP?4 (Catalog # ).

    • Source

      Mouse myeloma cell line, NS0-derived Gln28-Cys232

    • Accession #

    • N-terminal Sequence    
      Analysis

      No results obtained: Gln28 predicted    
       

    • Structure / Form

      Disulfide-linked homodimer    
       

    • Predicted Molecular Mass

      23 kDa (monomer)

    • SDS-PAGE

      30-33 kDa, reducing conditions

    Carrier Free

    What does CF mean?

    CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.

    What formulation is right for me?

    In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.

    6057-NG

     

    6057-NG/CF

    Formulation Lyophilized from a 0.2 μm filtered solution in PBS with BSA as a carrier protein.


    Formulation Lyophilized from a 0.2 μm filtered solution in PBS.

    Reconstitution Reconstitute at 250 μg/mL in PBS  containing at least 0.1% human or bovine serum albumin.


    Reconstitution Reconstitute at 250 μg/mL in PBS.

    Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.


    Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.

    Stability & Storage:       Use a manual defrost freezer and avoid repeated freeze-thaw cycles.      

    • 12 months from date of receipt, -20 to -70 °C as supplied.

    • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

    • 3 months, -20 to -70 °C under sterile conditions after reconstitution.


    Stability & Storage:       Use a manual defrost freezer and avoid repeated freeze-thaw cycles.      

    • 12 months from date of receipt, -20 to -70 °C as supplied.

    • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

    • 3 months, -20 to -70 °C under sterile conditions after reconstitution.

    Data Images

    Superior and Consistent Pluripotent Stem Cell Differentiation with R&D Systems Recombinant Human Noggin.      


           

    BG01V human embryonic stem cells were cultured in Mouse Embryonic Fibroblast Conditioned Media supplemented with FGF basic (5 ng/mL). Stem cells were driven into early cells of the neuroectoderm using a 3 day incubation in recombinant human Noggin (25 μg/mL) from either R&D Systems (Lot 1, Lot 2; Catalog #
    6057-NG) or from two separate competitors (Competitor 1, Competitor 2). Control cells were not incubated in Noggin (No Noggin). The cells were stained for the early ectoderm marker, Otx2, and the neuroectoderm marker, SOX1. (A) Representative images of SOX1 (green), Otx2 (red), and DAPI (blue) staining in embryonic stem cells differentiated with Noggin from R&D Systems or Noggin from Competitor 2. (B) SOX1+ clusters were quantified under each of the indicated culture conditions. Cells treated with R&D Systems Noggin showed an increase in SOX1+ cells compared to both untreated and competitor-treated cells. R&D Systems Noggin showed consistent differentiation across the lots tested. BG01V human embryonic stem cells are licensed from ViaCyte, Inc.

    Background: Noggin

    Noggin is a secreted homodimeric glycoprotein that is an antagonist of bone morphogenetic proteins (BMPs) (1, 2). Human Noggin cDNA encodes a 232 amino acid (aa) precursor protein; cleavage of a 19 aa signal peptide generates the 213 aa mature protein which contains an N-terminal acidic region, a central basic heparin?binding segment and a C-terminal cysteine-knot structure (2). Secreted Noggin probably remains close to the cell surface due to its binding of heparin?containing proteoglycans (3). Noggin is very highly conserved among vertebrates, such that mature human Noggin shares 99%, 99%, 98%, 97% and 89% aa sequence identity with mouse, rat, bovine, equine and chicken Noggin, respectively. Noggin binds some BMPs such as BMP-4 with high affinity and others such as BMP-7 with lower affinity. It antagonizes BMP bioactivities by blocking epitopes on BMPs that are needed for binding to both type I and type II receptors (2, 4). During embryogenesis, Noggin antagonizes specific BMPs at defined times, for example, during neural tube, somite and cardiomyocyte growth and patterning (5-7). During skeletal development, Noggin prevents chondrocyte hyperplasia, thus allowing proper formation of joints (4). Mutations within the cysteine-knot region of human Noggin are linked to multiple types of skeletal dysplasias that result in apical joint fusions (8). Noggin is expressed in defined areas of the adult central nervous system and peripheral tissues such as lung, skeletal muscle and skin (1). During culture of human embryonic stem cells (hESC) or neural stem cells under certain conditions, addition of Noggin to antagonize BMP activity may allow stem cells to proliferate while maintaining their undifferentiated state, or alternatively, to differentiate into dopaminergic neurons (6, 9 - 13). Noggin also appears to maintain adult stem cell populations in-vivo, for example, maintaining neural stem cells within the hippocampus (13).

    • References:

      1. Valenzuela, D.M. et al. (1995) J. Neurosci. 15:6077.

      2. Groppe, J. et al. (2002) Nature 420:636.

      3. Paine-Saunders, S et al. (2002) J. Biol. Chem. 277:2089.

      4. Brunet, L. J. et al. (1998) Science 280:1455.

      5. McMahon, J. A. et al. (1998) Genes Dev. 12:1438.

      6. Itsykson, P. et al. (2005) Mol. Cell. Neurosci. 30:24.

      7. Yuasa, S. et al. (2005) Nat. Biotechnol. 23:607.

      8. Gong, Y. et al. (1999) Nat. Genet. 21:302.

      9. Xu, R.-H. et al. (2005) Nat. Methods 2:185.

      10. Wang, G. et al. (2005) Biochem. Biophys. Res. Commun. 330:934.

      11. Chaturvedi, G. et al. (2009) Cell Prolif. 42:425.

      12. Chiba, S. et al. (2008) Stem Cells 26:2810.

      13. Bonaguidi, M.A. et al. (2008) J. Neurosci. 28:9194.

    • Entrez Gene IDs:

      9241 (Human); 18121 (Mouse)

    • Alternate Names:

      NOG; Noggin; SYM1; symphalangism 1 (proximal); synostoses (multiple) syndrome 1; SYNS1








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