Recombinant Rat Methyl-CpG-binding protein 2 (Mecp2)
-
中文名称:大鼠Mecp2重组蛋白
-
货号:CSB-YP013638RA
-
规格:
-
来源:Yeast
-
其他:
-
中文名称:大鼠Mecp2重组蛋白
-
货号:CSB-EP013638RA
-
规格:
-
来源:E.coli
-
其他:
-
中文名称:大鼠Mecp2重组蛋白
-
货号:CSB-EP013638RA-B
-
规格:
-
来源:E.coli
-
共轭: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:
-
中文名称:大鼠Mecp2重组蛋白
-
货号:CSB-BP013638RA
-
规格:
-
来源:Baculovirus
-
其他:
-
中文名称:大鼠Mecp2重组蛋白
-
货号:CSB-MP013638RA
-
规格:
-
来源:Mammalian cell
-
其他:
产品详情
-
纯度:>85% (SDS-PAGE)
-
基因名:
-
Uniprot No.:
-
别名:Mecp2Methyl-CpG-binding protein 2; MeCp-2 protein; MeCp2
-
种属:Rattus norvegicus (Rat)
-
蛋白长度:Full length protein
-
表达区域:1-492
-
氨基酸序列MVAGMLGLRK EKSEDQDLQG LKEKPLKFKK VKKDKKEDKE GKHEPLQPSA HHSAEPAEAG KAETSESSGS APAVPEASAS PKQRRSIIRD RGPMYDDPTL PEGWTRKLKQ RKSGRSAGKY DVYLINPQGK AFRSKVELIA YFEKVGDTSL DPNDFDFTVT GRGSPSRREQ KPPKKPKSPK APGTGRGRGR PKGSGTGRPK AAASEGVQVK RVLEKSPGKL LVKMPFQASP GGKGEGGGAT TSAQVMVIKR PGRKRKAEAD PQAIPKKRGR KPGSVVAAAA AEAKKKAVKE SSIRSVQETV LPIKKRKTRE TVSIEVKEVV KPLLVSTLGE KSGKGLKTCK SPGRKSKESS PKGRSSSASS PPKKEHHHHH HHAESPKAPM PLLPPPPPPE PQSSEDPISP PEPQDLSSSI CKEEKMPRAG SLESDGCPKE PAKTQPMVAA AATTTTTTTT TVAEKYKHRG EGERKDIVSS SMPRPNREEP VDSRTPVTER VS
-
蛋白标签: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. -
产品提供形式: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. -
复溶: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.
-
储存条件:Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
-
保质期: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. -
货期: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.
-
注意事项: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.
靶点详情
-
功能:Chromosomal protein that binds to methylated DNA. It can bind specifically to a single methyl-CpG pair. It is not influenced by sequences flanking the methyl-CpGs. Mediates transcriptional repression through interaction with histone deacetylase and the corepressor SIN3A. Binds both 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC)-containing DNA, with a preference for 5-methylcytosine (5mC).
-
基因功能参考文献:
- MeCP2 directly binds to MBP, PLP, and BDNF promoter in oligodendrocytes. MeCP2 differentially regulates the myelin gene expression in oligodendrocytes and C6 glioma. PMID: 29992497
- These data reveal a functional role of miR-218 and its target, MeCP2, in the regulation of heroin-induced behavioral plasticity. PMID: 28074855
- in adjuvant arthritis fibroblast-like synoviocytes, MeCP2 mediates hypermethylation of PTCH1 gene and decreases the expression of PTCH1 protein, thus activating Hedgehog signaling pathway and increasing secretion of IL-6 and TNF-alpha. PMID: 28573530
- Motor, somatosensory, viscerosensory and metabolic impairments in a heterozygous Mecp2-deficient female rat model of Rett Syndrome. PMID: 29286317
- site-specific methylation and MeCP2 are required for maintenance of basal levels of CRH gene expression. PMID: 28655627
- This study showed that epigenetic regulation of gene expression by MeCP2 may differentially influence the motivational effects of Methamphetamine and natural reinforcement. PMID: 27312406
- these findings demonstrate that the Mecp2 rat model is a complementary tool with unique features for the study of Rett syndrome and highlight the potential benefit of cross-species analyses in identifying potential disease-relevant preclinical outcome measures PMID: 27365498
- MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats PMID: 27329765
- work suggests that a feedback regulatory mechanism involving both miR-130a and MeCP2 may serve to ensure their appropriate expression and function in neural development. PMID: 27245166
- This study demonstrated that the MeCP2 and diverse pMeCP2s have distinct features of spatio-temporal expression in the rat brain, and that the precise levels of MeCP2 in the postnatal period are vital to cerebellar neural cell development. PMID: 27995568
- We demonstrated that MeCP2 may negatively control the acetylation of alpha-tubulin through HDAC6 in cardiac fibroblast proliferation and fibrosis PMID: 26975406
- MeCP2 acts as a key regulator of pathological cardiac fibrosis, promotes cardiac fibroblasts proliferation and fibrosis by down-regulation of DUSP5. PMID: 26511729
- DNMT1 activates the canonical Wnt signaling in rheumatoid arthritis model rats via a crucial functional crosstalk between miR-152 and the DNMT1, MeCP2 PMID: 26093272
- homeostatic interactions between MeCP2 and miR132 may regulate hippocampal BDNF levels, which may have a role in the pathogenesis of MDD. PMID: 26239616
- Results together reveal an important role of MeCP2 SUMOylation in social interaction, memory and synaptic plasticity, and that abnormal MeCP2 SUMOylation is implicated in Rett syndrome. PMID: 26842955
- MeCP2 knockdown in cultured oligodendrocytes increased myelin genes expression. PMID: 26140854
- induction of miR-132/212 following bladder outlet obstruction: association with MeCP2 repression and cell viability PMID: 25617893
- Results show that overexpression of VEGF enhances accumulation of pS292 MeCP2 in reactive astrocytes in ischemic-injured rat striatum, implicating a pS292 MeCP2-related epigenetic role of exogenous VEGF in reactive astrocytes following cerebral ischemia PMID: 25511996
- A long-lasting increase in MeCP2 expression was found throughout the striatum of maternally deprived rats compared to controls. PMID: 23980619
- Results suggest that fetal alcohol programming of POMC gene may involve recruitment of MeCP2 on to the methylated promoter of the POMC gene to suppress POMC transcript levels and contribute to hypothalamic-pituitary-adrenal axis dysregulation. PMID: 25409090
- Passive and voluntary cocaine administration positively regulate Mecp2 and negatively PP1Cbeta protein expression in reward-related brain structures; the two proteins were induced by food operant conditioning, no effect when food was passively delivered PMID: 24936739
- MeCp2 direct repression of GluA1 function in amygdala is a likely mechanism for morphine-seeking behavior maintained by long-lasting affective pain after morphine withdrawal. PMID: 25716866
- These data contribute to the idea that the role of MeCP2 differs in the developing male versus female brain. Further elucidating the regulation and function of GFAP can contribute to our understanding of MeCP2 function. PMID: 24269336
- data demonstrate that PP1Cbeta is a direct MeCP2-target gene in vivo. PMID: 23688924
- The SUMOylation of MeCP2 at K223 is a critical switch for transcriptional repression and plays a crucial function in regulating synaptic development in the central nervous system. PMID: 24188180
- MeCP2 binding triggers the loss of HP1gamma at the chromosomal domain and an increased HP1gamma mobility. PMID: 23935992
- MeCP2 controls PTCH1 expression during Hepatic stellate cell activation and proliferation. PMID: 23333245
- MeCP2 and DNA methylation may provide molecular mechanisms for canonical Wnt pathway activation in Rheumatoid arthritis. PMID: 23200852
- Results suggest that changes in chromatin compaction, regulated by the binding of MeCP2 complexes to methylated DNA, are involved in the modulation of gene expression in the superficial dorsal horn and dorsal root ganglia during persistent pain states. PMID: 22369085
- MeCP2 is a multifuncitonal protein with a role in mRNA biogenesis, using an additional mechanism for Rett syndrome pathophysiology. PMID: 21070191
- We demonstrated the presence of MeCP2 mRNA, protein, and miR132 in the rat lung throughout alveolarization. PMID: 21425435
- MeCP2 and DNA methylation may provide molecular mechanisms for perpetuated fibroblast activation and fibrogenesis in the liver PMID: 22056649
- MeCP2 is essential for myofibroblast differentiation and pulmonary fibrosis PMID: 21435439
- A very clear presence of MeCP2 protein is found in oligodendrocyte progenitors isolated from neonatal rat brain. PMID: 20697302
- MeCP2 regulates cocaine intake through homeostatic interactions with miR-212 to control the effects of cocaine on striatal BDNF levels, these interactions may be important in regulating vulnerability to cocaine addiction PMID: 20711185
- Cdkl5 is a MeCP2-repressed target gene providing a link between genes the mutation of which generates overlapping symptoms: DNA methylation changes are a potential mechanism participating in the long-term plasticity triggered by pharmacological agents PMID: 20211261
- MeCP2 associates with DNA methyltransferase /Dnmt1/ in order to perform maintenance DNA methylation in vivo PMID: 12473678
- MeCP2 plays arole in neuronal maturation, and/or the maintence of neurons in a differentiated state. PMID: 12605461
- MeCP2 protein expression has a role in the initiation and/or progression of hepatic cancer induced by methyl deficiency PMID: 12949043
- findings show that MeCP2 binds selectively to BDNF promoter III and functions to repress expression of the BDNF gene PMID: 14593183
- MeCP2 expression is correlated with synaptogenesis is consistent with the hypothesis that Rett Syndrome is caused by defects in the formation or maintenance of synapses. PMID: 14751287
- Highest MeCP2 expression was in olfactory bulb and frontal cortex. Little was detected in caudate-putamen, septum and hippocampus. Except in the olfactive nuclei, very few cells showed detectable MeCP2 at birth. PMID: 15006690
- MeCP2 is an elongated monomer that does not stably associate with the Sin3a chromatin remodeling complex PMID: 15322089
- MeCP2 and DNA methylation exert epigenetic control over hepatic wound healing and fibrogenesis. PMID: 16763620
- By triggering MeCP2 phosphorylation, neuronal activity regulates a program of gene expression that mediates CNS maturation and distruption of this process in individuals with mutations in MeCP2 may underlie the neural-specific pathology of RTT. PMID: 17046689
- Phosphorylation of MeCP2 regulates activity-dependent gene transcription; MeCP2 is found to be phosphorylated in dorsal horn cells after peripheral inflammation. PMID: 17553988
- Results show that Bdnf mRNA expression decreased in the hippocampus, supporting the hypothesis that Bdnf may be a target gene of MeCP2 in the CNS. PMID: 18396005
- Report that clinically relevant concentrations of valproic acid modulate melatonin MT(1) receptor, HDAC and MeCP2 mRNA expression in C6 glioma cells. PMID: 18550052
- Mecp2 may have an overlooked role in the organization of sexually dimorphic behaviors and that male juvenile behavior is particularly sensitive to Mecp2 disruption during this period of development. PMID: 18614683
- These data indicate that DNA methylation as well as subsequent MeCP2 association mediates neuronal activity-dependent regulation of NR2B expressions. PMID: 18952054
显示更多
收起更多
-
亚细胞定位:Nucleus.
-
组织特异性:Present in all adult somatic tissues tested.
-
数据库链接:
KEGG: rno:29386
STRING: 10116.ENSRNOP00000053166
UniGene: Rn.38416
Most popular with customers
-
Recombinant Human Leukemia inhibitory factor receptor (LIFR), partial (Active)
Express system: Mammalian cell
Species: Homo sapiens (Human)
-
Recombinant Human Angiopoietin-2 (ANGPT2) (Active)
Express system: Mammalian cell
Species: Homo sapiens (Human)
-
Recombinant Rat Intestinal-type alkaline phosphatase 1 (Alpi) (Active)
Express system: Mammalian cell
Species: Rattus norvegicus (Rat)
-
Recombinant Mouse Tyrosine-protein kinase Mer (Mertk), partial (Active)
Express system: Mammalian cell
Species: Mus musculus (Mouse)
-
Recombinant Human Glucagon-like peptide 1 receptor (GLP1R), partial (Active)
Express system: Mammalian cell
Species: Homo sapiens (Human)
-
Recombinant Human C-C chemokine receptor type 8 (CCR8)-VLPs (Active)
Express system: Mammalian cell
Species: Homo sapiens (Human)
-
Recombinant Human Serine/threonine-protein kinase receptor R3 (ACVRL1), partial (Active)
Express system: Baculovirus
Species: Homo sapiens (Human)
-
Recombinant Human CD81 antigen (CD81), partial (Active)
Express system: Mammalian cell
Species: Homo sapiens (Human)