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首頁 > 抗體 > 一抗 > 其它 > Rsk-2 Monoclonal Antibody
Rsk-2 Monoclonal Antibody
商品貨號: PLA005022
適 應 性:
WB IF ELISA FCM
¥600元
規(guī)格:
在線咨詢
MSDS
說明書
商品描述
  • 發(fā)貨日期: 7
  • 基因名稱: RPS6KA3
  • 蛋白名稱: Ribosomal protein S6 kinase alpha-3
  • Human_gene_id: 6197
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6197
  • Human_swiss_prot_no: P51812
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P51812/entry
  • Mouse_swiss_prot_no: P18654
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P18654
  • 特異性: Rsk-2 Monoclonal Antibody detects endogenous levels of Rsk-2 protein.
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Monoclonal, Mouse
  • 稀釋: WB 1:500 - 1:2000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
  • 純化工藝: Affinity purification
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名稱: RPS6KA3; ISPK1; MAPKAPK1B; RSK2; Ribosomal protein S6 kinase alpha-3; S6K-alpha-3; 90 kDa ribosomal protein S6 kinase 3; p90-RSK 3; p90RSK3; Insulin-stimulated protein kinase 1; ISPK-1; MAP kinase-activated protein kinase 1b; MAPK-activated
  • 信號通路: Regulates Angiogenesis; Insulin Receptor; B Cell Receptor; AMPK
  • 功能: catalytic activity:ATP + a protein = ADP + a phosphoprotein.,cofactor:Magnesium.,disease:Defects in RPS6KA3 are the cause of Coffin-Lowry syndrome (CLS) [MIM:303600]; an X-linked dominant disorder characterized by severe mental retardation with facial and digital dysmorphisms, and progressive skeletal deformations.,enzyme regulation:Activated by multiple phosphorylations on threonine and serine residues.,function:Serine/threonine kinase that may play a role in mediating the growth-factor and stress induced activation of the transcription factor CREB.,PTM:Autophosphorylated on Ser-386, as part of the activation process.,PTM:Ser-227 phosphorylation promotes Ser-386 phosphorylation and leads to basal activation. Full activation by growth factors requires additional phosphorylation on Ser-369.,similarity:Belongs to the protein kinase superfamily. AGC Ser/Thr protein kinase family. S6 kinase subfamily.,similarity:Contains 1 AGC-kinase C-terminal domain.,similarity:Contains 2 protein kinase domains.,subunit:Forms a complex with either ERK1 or ERK2 in quiescent cells. Transiently dissociates following mitogenic stimulation (By similarity). Interacts with NFATC4.,tissue specificity:Expressed in many tissues, highest levels in skeletal muscle.,
  • 相關產(chǎn)品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Nucleus . Cytoplasm .
  • 組織表達: Expressed in many tissues, highest levels in skeletal muscle.
  • 科研貨號: PLA005022
Rsk-2 Monoclonal Antibody
Catalog No PLA005022
Product information
  • 發(fā)貨日期: 7
  • 基因名稱: RPS6KA3
  • 蛋白名稱: Ribosomal protein S6 kinase alpha-3
  • Human_gene_id: 6197
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6197
  • Human_swiss_prot_no: P51812
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P51812/entry
  • Mouse_swiss_prot_no: P18654
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P18654
  • 特異性: Rsk-2 Monoclonal Antibody detects endogenous levels of Rsk-2 protein.
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Monoclonal, Mouse
  • 稀釋: WB 1:500 - 1:2000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
  • 純化工藝: Affinity purification
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名稱: RPS6KA3; ISPK1; MAPKAPK1B; RSK2; Ribosomal protein S6 kinase alpha-3; S6K-alpha-3; 90 kDa ribosomal protein S6 kinase 3; p90-RSK 3; p90RSK3; Insulin-stimulated protein kinase 1; ISPK-1; MAP kinase-activated protein kinase 1b; MAPK-activated
  • 信號通路: Regulates Angiogenesis; Insulin Receptor; B Cell Receptor; AMPK
  • 功能: catalytic activity:ATP + a protein = ADP + a phosphoprotein.,cofactor:Magnesium.,disease:Defects in RPS6KA3 are the cause of Coffin-Lowry syndrome (CLS) [MIM:303600]; an X-linked dominant disorder characterized by severe mental retardation with facial and digital dysmorphisms, and progressive skeletal deformations.,enzyme regulation:Activated by multiple phosphorylations on threonine and serine residues.,function:Serine/threonine kinase that may play a role in mediating the growth-factor and stress induced activation of the transcription factor CREB.,PTM:Autophosphorylated on Ser-386, as part of the activation process.,PTM:Ser-227 phosphorylation promotes Ser-386 phosphorylation and leads to basal activation. Full activation by growth factors requires additional phosphorylation on Ser-369.,similarity:Belongs to the protein kinase superfamily. AGC Ser/Thr protein kinase family. S6 kinase subfamily.,similarity:Contains 1 AGC-kinase C-terminal domain.,similarity:Contains 2 protein kinase domains.,subunit:Forms a complex with either ERK1 or ERK2 in quiescent cells. Transiently dissociates following mitogenic stimulation (By similarity). Interacts with NFATC4.,tissue specificity:Expressed in many tissues, highest levels in skeletal muscle.,
  • 相關產(chǎn)品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Nucleus . Cytoplasm .
  • 組織表達: Expressed in many tissues, highest levels in skeletal muscle.
  • 科研貨號: PLA005022
  • Hunan UPT Biotechnology Co.,Ltd
    Website:m.hyjdss.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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