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          上海雅吉生物科技有限公司>資料下載>磷酸化α型-過氧化酶活化增生受體抗體文獻引用

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          磷酸化α型-過氧化酶活化增生受體抗體文獻引用

          閱讀:440          發(fā)布時間:2019-8-19
          提 供 商 上海雅吉生物科技有限公司 資料大小 33.2KB
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          英文名稱phospho-PPAR alpha (Ser12)
          中文名稱磷酸化α型-過氧化酶活化增生受體抗體
          別    名PPAR alpha (phospho-Ser12); PPAR alpha (phospho-S12); p-PPAR alpha (Ser12); p-PPAR alpha (S12); hPPAR; MGC2237; MGC2452; NR1C1; Nuclear receptor subfamily 1 group C member 1; Peroxisome Proliferator Activated Receptor alpha; PPAR; PPAR alpha; PPARA; OTTHUMP00000197740; OTTHUMP00000197741; Peroxisome proliferator-activated receptor alpha; PPAR-alpha; PPARA_HUMAN; PPARalpha.  
          說 明 書100ul  
          產(chǎn)品類型磷酸化抗體 
          研究領(lǐng)域腫瘤  細胞生物  免疫學  轉(zhuǎn)錄調(diào)節(jié)因子  激酶和磷酸酶  
          抗體來源Rabbit
          克隆類型Polyclonal
          交叉反應(yīng)Human, Mouse, Rat, Dog, Pig, Cow, Horse, Guinea Pig, 
          產(chǎn)品應(yīng)用WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:100-500 (石蠟切片需做抗原修復(fù)) 
          not yet tested in other applications.
          optimal dilutions/concentrations should be determined by the end user.
          分 子 量52kDa
          細胞定位細胞核 
          性    狀Lyophilized or Liquid
          濃    度1mg/ml
          免 疫 原KLH conjugated Synthesised phosphopeptide derived from human PPAR alpha around the phosphorylation site of ser12:PL(p-S)PL 
          亞    型IgG
          純化方法affinity purified by Protein A
          儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
          保存條件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
          PubMedPubMed
          產(chǎn)品介紹background:
          Peroxisome proliferators are nongenotoxic carcinogens which are purported to exert their effect on cells through their interaction with members of the nuclear hormone receptor family, termed Peroxisome Proliferator Activated Receptors (PPARs). Nuclear hormone receptors are ligand dependent intracellular proteins that stimulate transcription of specific genes by binding to specific DNA sequences following activation by the appropriate ligand. Studies indicate that PPARs are activated by peroxisome proliferators such as clofibric acid, nafenopin, and WY-14,643, as well as by some fatty acids. It has also been shown that PPARs can induce transcription of acyl coenzyme A oxidase and cytochrome P450 A6 (CYP450 A6) through interaction with specific response elements. PPAR alpha is activated by free fatty acids including linoleic, arachidonic, and oleic acids. Induction of peroxisomes by this mechanism leads to a reduction in blood triglyceride levels. PPAR alpha is expressed mainly in skeletal muscle, heart, liver, and kidney and is thought to regulate many genes involved in the beta-oxidation of fatty acids. Activation of rat liver PPAR alpha has been shown to suppress hepatocyte apoptosis. PPAR alpha, like several other nuclear hormone receptors, heterodimerizes with retinoic X receptor (RXR) alpha to form a transcriptionally competent complex.

          Function:
          Ligand-activated transcription factor. Key regulator of lipid metabolism. Activated by the endogenous ligand 1-palmitoyl-2-oleoyl-sn-glycerol-3-phosphocholine (16:0/18:1-GPC). Activated by oleylethanolamide, a naturally occurring lipid that regulates satiety (By similarity). Receptor for peroxisome proliferators such as hypolipidemic drugs and fatty acids. Regulates the peroxisomal beta-oxidation pathway of fatty acids. Functions as transcription activator for the ACOX1 and P450 genes. Transactivation activity requires heterodimerization with RXRA and is antagonized by NR2C2.

          Subunit:
          Heterodimer; with RXRA. This heterodimerization is required for DNA binding and transactivation activity. Interacts with AKAP13, LPIN1 and PRDM16. Also interacts with PPARBP coactivator in vitro. Interacts with CITED2; the interaction stimulates its transcriptional activity (By similarity). Interacts with NCOA3 and NCOA6 coactivators. Interacts with ASXL1 AND ASXL2.

          Subcellular Location:
          Nucleus.

          Tissue Specificity:
          Skeletal muscle, liver, heart and kidney.

          Similarity:
          Belongs to the nuclear hormone receptor family. NR1 subfamily. 
          Contains 1 nuclear receptor DNA-binding domain.

          SWISS:
          Q07869

          Gene ID:
          5465

          Database links:
          Entrez Gene: 5465 Human

          Entrez Gene: 19013 Mouse

          Entrez Gene: 25747 Rat

          Omim: 170998 Human

          SwissProt: Q07869 Human

          SwissProt: Q6I9S0 Human

          SwissProt: P23204 Mouse

          SwissProt: Q542P9 Mouse

          SwissProt: P37230 Rat

          Unigene: 103110 Human

          Unigene: 710044 Human

          Unigene: 212789 Mouse

          Unigene: 9753 Rat


          Important Note:
          This product as supplied is intended for research use only, not for use in human, therapeutic or di

          產(chǎn)品圖片

          Sample: 
          Liver (Rat) Lysate at 40 ug
          Primary: Anti-phospho-PPAR alpha (Ser12) (bs-4055R) at 1/300 dilution
          Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
          Predicted band size: 52 kD
          Observed band size: 52 kD

          Sample: 
          Heart (Mouse) Lysate at 40 ug
          Liver (Mouse) Lysate at 40 ug
          Primary: Anti-phospho-PPAR alpha (Ser12) (bs-4055R) at 1/300 dilution
          Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
          Predicted band size: 52 kD
          Observed band size: 52 kD

          Sample: 
          Colon carcinoma (Human) Lysate at 40 ug
          Embryo (Mouse) Lysate at 40 ug
          Primary: Anti- phospho-PPAR alpha (Ser12) (bs-4055R) at 1/300 dilution
          Secondary: HRP conjugated Goat-Anti-rabbit IgG (bs-0295G-HRP) at 1/5000 dilution
          Predicted band size: 52 kD
          Observed band size: 52 kD

          Tissue/cell: rat kidney tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; 
          Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; 
          Incubation: Anti-phospho-PPAR alpha(Ser12) Polyclonal Antibody, Unconjugated(bs-4055R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining

          phosphopeptide non phosphopeptide

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