Recombinant Mouse Fibrillin-1 (Fbn1), partial

中文名稱：

小鼠Fbn1重組蛋白
貨號：

CSB-YP736825MO
說明書：

MSDS Datasheet
規(guī)格：
來源：

Yeast
其他：

中文名稱：

小鼠Fbn1重組蛋白
貨號：

CSB-EP736825MO
說明書：

MSDS Datasheet
規(guī)格：
來源：

E.coli
其他：

中文名稱：

小鼠Fbn1重組蛋白
貨號：

CSB-EP736825MO-B
說明書：

MSDS Datasheet
規(guī)格：
來源：

E.coli
共軛：

Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
其他：

中文名稱：

小鼠Fbn1重組蛋白
貨號：

CSB-BP736825MO
說明書：

MSDS Datasheet
規(guī)格：
來源：

Baculovirus
其他：

中文名稱：

小鼠Fbn1重組蛋白
貨號：

CSB-MP736825MO
說明書：

MSDS Datasheet
規(guī)格：
來源：

Mammalian cell
其他：

產(chǎn)品詳情
產(chǎn)品評價
靶點詳情

產(chǎn)品詳情

純度：

>85% (SDS-PAGE)
基因名：

Fbn1
Uniprot No.：

Q61554
別名：

Fbn1; Fbn-1Fibrillin-1 [Cleaved into: Asprosin]
種屬：

Mus musculus (Mouse)
蛋白長度：

Partial
蛋白標簽：

Tag?type?will?be?determined?during?the?manufacturing?process.

The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
產(chǎn)品提供形式：

Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
復溶：

We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
儲存條件：

Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
保質期：

The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
貨期：

Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
注意事項：

Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Datasheet ：

Please contact us to get it.

產(chǎn)品評價

靶點詳情

功能：

Structural component of the 10-12 nm diameter microfibrils of the extracellular matrix, which conveys both structural and regulatory properties to load-bearing connective tissues. Fibrillin-1-containing microfibrils provide long-term force bearing structural support. In tissues such as the lung, blood vessels and skin, microfibrils form the periphery of the elastic fiber, acting as a scaffold for the deposition of elastin. In addition, microfibrils can occur as elastin-independent networks in tissues such as the ciliary zonule, tendon, cornea and glomerulus where they provide tensile strength and have anchoring roles. Fibrillin-1 also plays a key role in tissue homeostasis through specific interactions with growth factors, such as the bone morphogenetic proteins (BMPs), growth and differentiation factors (GDFs) and latent transforming growth factor-beta-binding proteins (LTBPs), cell-surface integrins and other extracellular matrix protein and proteoglycan components. Regulates osteoblast maturation by controlling TGF-beta bioavailability and calibrating TGF-beta and BMP levels, respectively. Negatively regulates osteoclastogenesis by binding and sequestering an osteoclast differentiation and activation factor TNFSF11. This leads to disruption of TNFSF11-induced Ca(2+) signaling and impairment of TNFSF11-mediated nuclear translocation and activation of transcription factor NFATC1 which regulates genes important for osteoclast differentiation and function. Mediates cell adhesion via its binding to cell surface receptors integrins ITGAV:ITGB3 and ITGA5:ITGB1. Binds heparin and this interaction plays an important role in the assembly of microfibrils.; Adipokine secreted by white adipose tissue that plays an important regulatory role in the glucose metabolism of liver, muscle and pancreas. Hormone that targets the liver in response to fasting to increase plasma glucose levels. Binds the olfactory receptor Olfr734 at the surface of hepatocytes and promotes hepatocyte glucose release by activating the protein kinase A activity in the liver, resulting in rapid glucose release into the circulation. May act as a regulator of adaptive thermogenesis by inhibiting browning and energy consumption, while increasing lipid deposition in white adipose tissue. Also acts as an orexigenic hormone that increases appetite: crosses the blood brain barrier and exerts effects on the hypothalamus. In the arcuate nucleus of the hypothalamus, asprosin directly activates orexigenic AgRP neurons and indirectly inhibits anorexigenic POMC neurons, resulting in appetite stimulation. Activates orexigenic AgRP neurons via binding to the olfactory receptor Olfr734. May also play a role in sperm motility in testis via interaction with Olfr734 receptor.
基因功能參考文獻：
1. The abundance of elastic fibers was reduced and fragmented in obesity, suggesting that the reduction in elastic fibers is initially caused by increased neprilysin and decreased fibrillin-1 expression, which may inhibit formation and stabilization of elastic fibers, resulting in skin fragility in obesity. PMID: 27892729
2. fibrillin-1 contributes little to lipid storage and metabolic homeostasis, which is in contrast to the obesity and metabolic changes associated with MAGP1 deficiency. PMID: 26902431
3. In young Fbn1(C1039G/+) mice, aortopathy develops in the absence of detectable alterations in smooth muscle cell (SMC) TGF-beta signaling. Loss of physiologic SMC TGF-beta signaling exacerbates MFS-associated aortopathy. Our data support a protective role for SMC TGF-beta signaling during early development of MFS-associated aortopathy. PMID: 28119285
4. Studies of Marfan syndrome and congenital contractural arachnodactyly mice have correlated the skeletal phenotypes of these mutant animals with distinct pathophysiological mechanisms that reflect the contextual contribution of fibrillin-1 and -2 scaffolds to TGFbeta and BMP signaling during bone patterning, growth and metabolism. [review] PMID: 26408953
5. Findings demonstrate that loss of fibrillin-1 in the mouse's marrow causes significant hematopoietic abnormalities, such as hematopoietic stem cell (HSC) depletion and augmented erythropoiesis (polycythemia). Furthermore, the distinct outcomes of systemic TGFbeta neutralization in mutant mice strongly suggest that fibrillin-1 differentially modulates TGFbeta signaling within HSC and erythroid niches. PMID: 26610678
6. This study shows that Raman microspectroscopy is able to reveal structural changes in fibrillin-1 microfibrils and elastic fiber networks and to discriminate between normal and diseased networks in vivo and in vitro. PMID: 27956365
7. Resveratrol inhibits aortic root dilatation in Fbn1C1039G/+ Marfan mice by promoting elastin integrity and smooth muscle cell survival, involving downregulation of the aneurysm-related micro-RNA-29b in the aorta. PMID: 27283746
8. These results suggest that both fibrillin-1 and fibrillin-2 expression is required to form thick oxytalan fibers in periodontal ligament. PMID: 25524144
9. findings show that fibrillin-1 regulates MSC activity by modulating TGFbeta bioavailability within the microenvironment of marrow niches. PMID: 26189658
10. Fibrillin-1 mgDelta(lpn) Marfan syndrome mutation associates with preserved proteostasis and bypass of a protein disulfide isomerase-dependent quality checkpoint PMID: 26718974
11. fibrillin-1 deficiency is associated with relevant dysfunction of the endothelial barrier that enables adenovirus to induce vessel-harming inflammation. PMID: 26840980
12. the Fbn1(C1039G/+) mouse model demonstrates mild intrinsic left ventricular dysfunction PMID: 26042521
13. This study demonstrated that dysfunctional fibrillin-1 impairs blood-brain barrier permeability /BCSFB integrity, facilitating peripheral leukocyte infiltration, which further degrades the BBB/BCSFB. PMID: 25797463
14. The review discuss FBN1 point mutations on the structure and function of the protein associated with Marfan syndrome in affected patients impairing protein folding and traficking, secretion, proteolysis or heparin binding. PMID: 26281765
15. The concomitant induction of both fibrillin-1 and alpha8 integrin in a self-limited model of glomerular injury points to a protective role of the interaction of fibrillin-1 with alpha8 integrin in the glomerulus. PMID: 25482639
16. Data show that fibrillin-1 (FBN1) modulates bone marrow mesenchymal stem cells (BMMSCs) lineage differentiation via IL4 receptor alpha/mTOR protein signaling. PMID: 25534817
17. latent transforming growth factor-beta-1 binding protein-2 was prominently associated with annular fibrils containing fibrillin-1 PMID: 24867584
18. Activation of IL-6-STAT3 signaling contributes to aneurysmal dilation in fibrillin-1 deficient mice through increased MMP-9 activity, aggravating extracellular matrix degradation. PMID: 24449804
19. We targeted mutations in Pkd1 and Fbn1. Double heterozygotes displayed an exacerbation of the typical Fbn1 heterozygous aortic phenotype. The basis of this genetic interaction results from upregulation of TGF-beta signaling caused by Pkd1 haploinsufficiency. PMID: 24071006
20. Report immunolocalization of fibrillin-1/perlecan in HS-deficient hspg2 exon 3 null mutant mouse intervertebral disc. PMID: 23104139
21. analysis of the global biomechanical and local cell-matrix deformation relationships in the aging and Marfan related Fbn1 mutated murine mitral valve PMID: 22984535
22. Data show that fibrillin-1 expression was intense in the ligamentum flavum from E16 through P0, with E17 appearing to be the stage with the greatest staining intensity. PMID: 22685574
23. ADAMTSL6beta has a role in fibrillin-1 microfibril formation PMID: 21880733
24. fibrillin-1 plays a predominantly greater role than fibrillin-2 in determining the material properties of bones PMID: 21440062
25. Data support the development of therapies based on increasing Fbn1 expression. PMID: 21152435
26. Tight-skinned (Tsk-/+) mice demonstrate abnormal "big fibrillin" expression (405 kDa)and chronic oxidative stress that contribute to mesenchymal trnasition and reduction in angiogenesis in a model of systemic sclerosis. PMID: 21160034
27. Data show that a cluster of 205 genes, including Fbn1, were selectively expressed by mouse cell lines of different mesenchymal lineages. PMID: 20551991
28. Fibrillin 1 is indispensable for normal tissue architecture and gene expression of periodontal ligaments. PMID: 20714769
29. Fibrillin-1 and -2, the structural components of extracellular microfibrils, differentially regulate TGF-beta and bone morphogenetic protein (BMP) bioavailability in bone. PMID: 20855508
30. analysis of mutant fibrillin-1 microfibrils PMID: 20529844
31. Results indicated that ADAMTSL-6 is a novel microfibril-associated protein that binds directly to fibrillin-1 and promotes fibrillin-1 matrix assembly. PMID: 19940141
32. interaction with microfibril-associated glycoprotein-2 PMID: 12122015
33. there is a molecular basis for compensation of one fibrillin (1 or 2) by the other during fetal life PMID: 12429739
34. relaxin does not regulate its mRNA and protein expression by human dermal fibroblasts and murine fetal skin. PMID: 12590922
35. mice deficient in fibrillin-1 have marked dysregulation of transforming growth factor-beta (TGF-beta) activation and signaling, resulting in apoptosis in the developing lung, in a model of Marfan syndrome PMID: 12598898
36. Tight skin fibrillin 1 altered extracellular matrix organization and caused fibrosis by affecting deposition of MAGP-2 or other fibrillin-1-associated proteins. PMID: 15022335
37. Data are consistent with a model that invokes haploinsufficiency for wild type fibrillin-1, rather than production of mutant protein, as the primary determinant of failed microfibrillar assembly in Marfan syndrome. PMID: 15254584
38. High affinity interactions between fibrillin-1 and perlecan were found by kinetic binding studies with dissociation constants in the low nanomolar range. PMID: 15657057
39. ANG II can directly induce fibrillin-1 expression in cardiac fibroblasts PMID: 15849235
40. fibrillin-1 may contribute to glomerular damage in hypertensive and diabetic kidney disease PMID: 16380460
41. involvement of fibrillin-2 in the initial assembly of the aortic matrix overlaps in part with fibrillin-1 and continued fibrillin-1 deposition is absolutely required for the maturation and function of the vessel during neonatal life PMID: 16407178
42. Results suggest that changes in microfibril architecture brought about by fibrillin-1 mutation lead to a complex disease phenotype. PMID: 16488411
43. The distribution of Fbn1 was studied in the endometrium during estrus, diestrus, and pregnancy. PMID: 17587800
44. In Tsk mice the mutation in Fbn1 alters bone cell metabolism. PMID: 17705049
45. Fibrillin-1 microfibril deposition is dependent on fibronectin assembly. PMID: 18653538
46. Loss of fibrillin-1 deposition promotes the production of intracellular reactive oxygen species and abnormal accumulation of phosphorylated TGF-beta-activated kinase 1 and p38 MAPK in Marfan syndrome phenotype. PMID: 19109253
47. fibrillin-1, but not fibulin-2 or fibulin-4, is required for appropriate matrix assembly of latent transforming growth factor beta-binding proteins PMID: 19349279
48. The promoter region of the Fbn1 gene has been characterized. PMID: 19573590
49. Fragmentation of elastic fibers leads to increased vascular stiffness, which promotes features of multifocal plaque instability in atherosclerotic apolipopotein E-deficient mice with a mutated fibrillin 1 gene. PMID: 19948973
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亞細胞定位：

Secreted.; [Fibrillin-1]: Secreted, extracellular space, extracellular matrix.; [Asprosin]: Secreted.
蛋白家族：

Fibrillin family
組織特異性：

[Fibrillin-1]: Strongly expressed during the first week of osteoblast differentiation.; [Asprosin]: Secreted by white adipose tissue (at protein level).
數(shù)據(jù)庫鏈接：

KEGG: mmu:14118

STRING: 10090.ENSMUSP00000028633

UniGene: Mm.271644