Active Recombinant Human BMP7, Animal Free

Cat.No. : BMP7-135H
Product Overview : Recombinant human BMP-7 is a protein composed of 16.5 kDa single chain, containing 144 amino residues. Human recombinant protein expressed in Nicotiana benthamiana. Recombinant human BMP-7 contains a 6-His-tag at the N-terminal end, is produced by transient expression in non-transgenic plants and is purified by sequential chromatography (FPLC). This product contains no animal–derived components or impurities. Animal free product.
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Species : Human
Source : Nicotiana Benthamiana
Tag : Non
Protein Length : 144 a.a.
Description : The bone morphogenetic proteins are a family of secreted signalling molecules that can induce ectopic bone growth. BMPs were originally identified by an ability of demineralized bone extract to induce endochondral osteogenesis in vivo in an extraskeletal site. Bone morphogenetic protein 7 (BMP-7), also known as osteogenic protein 1 (OP1), is a widely expressed TGFb superfamily member with important functions during embryogenesis, in the adult, and in disease (Chen et al., 2004, Kishigami and Mishina 2005). BMP-7 plays a role in a variety of organ systems. It promotes new bone formation and nephron development (Sampath et al., 1992, Kazama et al., 2008), inhibits the branching of prostate epithelium (Grishina et al., 2005), and antagonizes epithelialmesenchymal transition (Zeisberg et al., 2003, Yu et al., 2009). In pathological conditions, BMP7 inhibits tumor growth and metastasis (Buijs et al., 2007), ameliorates fibrotic damage in nephritis (Zeisberg et al., 2003), and promotes neuroregeneration following brain ischemia (Chou et al., 2006).
Form : Lyophilized from a Tris HCl 0.05M buffer at pH 7.4.
Bio-activity : The biological activity of BMP-7 is measured by its ability to induce alkaline phosphatase production by ATDC5 cells. ED50 ≤ 40ng/ml
Molecular Mass : Recombinant human BMP-7 is a protein composed of 16.5 kDa single chain, containing 144 amino residues.
AA Sequence : HHHHHHSTGSKQRSQNRSKTPKNQEALRMANVAENSSSDQRQACKKHELYVSFRDLGWQDWIIAPEGYAAYYCEG ECAFPLNSYMNATNHAIVQTLVHFINPETVPKPCCAPTQLNAISVLYFDDSSNVILKKYRNMVVRACGCH
Endotoxin : < 0.04="" eu="" ug="" protein="" (lal="">
Purity : >97% by SDS-PAGE gel
Applications : Cell culture, Western blot
Storage : This lyophilized preparation is stable at 2-8o C for short term, long storage it should be kept at -20oC. Reconstituted protein should be stored in working aliquots at –20°C and it is recommended to add a carrier protein (0.1% HSA or BSA). Repeated freezing and thawing is not recommended.
Reconstitution : Lyophilized protein should be reconstituted in water to a concentration of 50 ng/ul. Upon reconstitution, It can be stored in working aliquots at –20°C for future use. Optimal reconstitution please follow batch Quality Control sheet instructions.
Gene Name BMP7 bone morphogenetic protein 7 [ Homo sapiens ]
Official Symbol BMP7
Synonyms BMP7; bone morphogenetic protein 7; OP 1; osteogenic protein 1; BMP-7; OP-1;
Gene ID 655
mRNA Refseq NM_001719
Protein Refseq NP_001710
MIM 112267
UniProt ID P18075
Chromosome Location 20q13
Pathway ALK2 signaling events, organism-specific biosystem; BMP receptor signaling, organism-specific biosystem; Cytokine-cytokine receptor interaction, organism-specific biosystem; Cytokine-cytokine receptor interaction, conserved biosystem; Endochondral Ossification, organism-specific biosystem; Hedgehog signaling pathway, organism-specific biosystem; Hedgehog signaling pathway, conserved biosystem;
Function cytokine activity; growth factor activity; protein binding; contributes_to protein binding;

Gremlin Promotes Peritoneal Membrane Injury in an Experimental Mouse Model and Is Associated with Increased Solute Transport in Peritoneal Dialysis Patients

Journal: The American Journal of Pathology    PubMed ID: 25194662    Data: 2015/11/1

Authors: Imad Siddique, Simon P. Curran, Peter J. Margetts

Article Snippet:In mice exposed to AdGrem1, we treated one group with 1D11 (a pan-specific TGF-β inhibitor provided by Genzyme Corp., Framingham, MA) at a dose of 10 mg/kg.In mice exposed to AdGrem1, we treated one group with 1D11 (a pan-specific TGF-β inhibitor provided by Genzyme Corp., Framingham, MA) at a dose of 10 mg/kg.. 24 A second group of mice exposed to AdGrem1 also received recombinant BMP7 (rBMP7) (Creative BioMart, Shirley, NY) at a dose of 300 μg/kg.. 25 Both 1D11 and rBMP7 were delivered on days 1, 3, and 5 post-infection with AdGrem1.25 Both 1D11 and rBMP7 were delivered on days 1, 3, and 5 post-infection with AdGrem1.

Histologic analysis of the anterior abdominal wall after exposure to AdDL or AdGrem1 in B6 mice. A: Normal peritoneal structure seen 7 days after AdDL. B–D: Increased submesothelial thickening and fibrosis 7, 14, and 21 days after exposure to AdGrem1. E: In animals treated with AdGrem1 and rBMP7, there is ongoing submesothelial thickening and angiogenesis. F: There is a decrease in submesothelial thickening in animals treated with AdGrem1 and 1D11. Sections were stained with Masson's trichrome. G–H: Quantitation of submesothelial histological examination in B6 mice exposed to AdDL or AdGrem1. G: Significantly increased submesothelial thickening is seen after exposure to AdGrem. The submesothelial thickening is significantly reduced by treatment with 1D11. H: Submesothelial angiogenesis seen in the peritoneal tissues of B6 mice exposed to AdGrem1 is not prevented by treatment with rBMP7 or 1D11. n = 4 for control (AdDL) group; n = 6 for treatment groups at each time point. Data are expressed as means ± SD (G and H). ?P < 0.05, ??P < 0.01, and ???P < 0.001. Original magnification: ×100 (A–F).

Histologic analysis of the anterior abdominal wall after exposure to AdDL or AdGrem1 in B6 mice. A: Normal peritoneal structure seen 7 days after AdDL. B–D: Increased submesothelial thickening and fibrosis 7, 14, and 21 days after exposure to AdGrem1. E: In animals treated with AdGrem1 and rBMP7, there is ongoing submesothelial thickening and angiogenesis. F: There is a decrease in submesothelial thickening in animals treated with AdGrem1 and 1D11. Sections were stained with Masson's trichrome. G–H: Quantitation of submesothelial histological examination in B6 mice exposed to AdDL or AdGrem1. G: Significantly increased submesothelial thickening is seen after exposure to AdGrem. The submesothelial thickening is significantly reduced by treatment with 1D11. H: Submesothelial angiogenesis seen in the peritoneal tissues of B6 mice exposed to AdGrem1 is not prevented by treatment with rBMP7 or 1D11. n = 4 for control (AdDL) group; n = 6 for treatment groups at each time point. Data are expressed as means ± SD (G and H). ?P < 0.05, ??P < 0.01, and ???P < 0.001. Original magnification: ×100 (A–F).

Adenovirus-mediated GREM1 overexpression is associated with decreased expression of BMP 7, BMP4, and E-cadherin (CDH1) in B6 mice. These effects are reversed by treatment with rBMP7 or 1D11. A: Representative Western blot analysis. Each lane represents protein from an individual mouse. Band density was normalized to α-tubulin (TUBA1A) and quantified in B–D. Increased gene expression of Col1a2 (E) and Vegf (F) seen in the peritoneal tissue of animals 7 days after treatment with AdGrem1; both of these effects are reversed by rBMP7 or 1D11. n = 4 for control (AdDL) group; n = 6 for treatment groups at each time point. Data are expressed as means ± SD (B–E). ?P < 0.05, ??P < 0.01, and ???P < 0.001.

Adenovirus-mediated GREM1 overexpression is associated with decreased expression of BMP 7, BMP4, and E-cadherin (CDH1) in B6 mice. These effects are reversed by treatment with rBMP7 or 1D11. A: Representative Western blot analysis. Each lane represents protein from an individual mouse. Band density was normalized to α-tubulin (TUBA1A) and quantified in B–D. Increased gene expression of Col1a2 (E) and Vegf (F) seen in the peritoneal tissue of animals 7 days after treatment with AdGrem1; both of these effects are reversed by rBMP7 or 1D11. n = 4 for control (AdDL) group; n = 6 for treatment groups at each time point. Data are expressed as means ± SD (B–E). ?P < 0.05, ??P < 0.01, and ???P < 0.001.

Evidence of EMT in peritoneal tissue. Sections stained for α smooth muscle actin (red, A–D), cytokeratin (green, E–H) and merged (I–L). A, E, and I: There is no evidence of EMT after infection with AdDL. B, F, and J: B6 mice demonstrate evidence of EMT with cells labeled with both α smooth muscle actin and cytokeratin (arrow). C, G, and K: Similar co-expression is seen in animals treated with AdGrem1 and rBMP7 (arrow). D, H, and L: Blockade of TGF-β using 1d11 prevents EMT. Blue – DAPI nuclear stain. M: Dual-labeled cells are quantified as noninvading (within the mesothelial cell layer) and invading (in the submesothelial zone). There is a significant decrease in EMT in AdGrem1-exposed animals treated with 1D11. n = 4 for control (AdDL) animals; n = 6 for treatment groups. Data are expressed as means ± SD (M). ?P < 0.05, ???P < 0.001. Original magnification: ×200 (A–L).

Evidence of EMT in peritoneal tissue. Sections stained for α smooth muscle actin (red, A–D), cytokeratin (green, E–H) and merged (I–L). A, E, and I: There is no evidence of EMT after infection with AdDL. B, F, and J: B6 mice demonstrate evidence of EMT with cells labeled with both α smooth muscle actin and cytokeratin (arrow). C, G, and K: Similar co-expression is seen in animals treated with AdGrem1 and rBMP7 (arrow). D, H, and L: Blockade of TGF-β using 1d11 prevents EMT. Blue – DAPI nuclear stain. M: Dual-labeled cells are quantified as noninvading (within the mesothelial cell layer) and invading (in the submesothelial zone). There is a significant decrease in EMT in AdGrem1-exposed animals treated with 1D11. n = 4 for control (AdDL) animals; n = 6 for treatment groups. Data are expressed as means ± SD (M). ?P < 0.05, ???P < 0.001. Original magnification: ×200 (A–L).

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