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- 详细信息
- 文献和实验
- 技术资料
- 服务名称:
PCR芯片
- 提供商:
SABio
| Product | Species | Technology | Cat. No. |
| PI3K-AKT Signaling Pathway PCR Array | Human | Gene Expression | PAHS-058Z |
| PI3K-AKT Signaling Pathway PCR Array | Mouse | Gene Expression | PAMM-058Z |
| PI3K-AKT Signaling Pathway PCR Array | Rat | Gene Expression | PARN-058Z |
| PI3K-AKT Signaling Pathway PCR Array | Zebrafish | Gene Expression | PAZF-058Z |
AKT and PI3K Family Members and Their Regulators: AKT1, AKT2, AKT3, BTK, GRB10, GRB2, HSPB1, ILK, MTCP1, PDK2, PDPK1, PIK3CA (p110a), PIK3CG, PIK3R1 (p85a), PIK3R2 (p85b), PAK1, PRKCA, PRKCB, PRKCZ, PTEN, TCL1A. IGF-1 Signaling Pathway: CSNK2A1, ELK1, FOS, GRB2, HRAS, IGF1, IGF1R, IRS1, JUN, MAP2K1, MAPK3, MAPK8, PTPN11, RAF1, RASA1, SHC1, SOS1, SRF. Inactivation of Gsk3 and the Accumulation of β-Catenin: ADAR, AKT1, APC, CCND1, CD14, CTNNB1, EIF2AK2, GJA1, GSK3B, IRAK1, MYD88, NFKB1, PDK1, TIRAP, TLR4, TOLLIP. PI3K Subunit p85 Genes and Regulation of Actin Organization and Cell Migration:CDC42, PDGFRA, RAC1, RHOA, WASL. PTEN Dependent Cell Cycle Arrest and Apoptosis: AKT1, CDKN1B (p27), FASLG, FOXO3, GRB2, ILK, ITGB1, MAPK1, MAPK3, PDK1, PDK2, PTEN, PTK2, RBL2, SHC1, SOS1. BAD Phosphorylation and Anti-apoptotic Pathways: AKT1, BAD, GRB2, HRAS, IGF1R, IRS1, MAP2K1, MAPK1, MAPK3, RAF1, RPS6KA1, SHC1, SOS1, YWHAH. Genes Involved in the mTOR Signaling Pathway: AKT1, EIF4B, EIF4E, EIF4EBP1, EIF4G1, FKBP1A, MTOR, PDK1, PDK2, PTEN, RHEB, RPS6KB1, TSC1, TSC2. Regulation of eIF4e and p70 S6 Kinase: AKT1, EIF4E, EIF4EBP1 (4E-BP1), EIF4G1, MTOR, IRS1, MAPK1, MAPK14, MAPK3, PABPC1, PDK1, PDK2, PRKCA, PTEN, RPS6KB1. Other Genes Involved in the AKT Signaling Pathway: CASP9, CHUK, FOXO1, NFKBIA.
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Wnt Signaling in the Early Sea Urchin Embryo
Wnt signaling regulates a remarkably diverse array of cellular and developmental events during animal embryogenesis and homeostasis. The crucial role that Wnt signaling plays in regulating axial patterning in early embryos
is made through the integration of the pathway of NF-κB activation with a complex array of cell signaling networks that are at present poorly understood. Here, two methods are presented, protein co-immunoprecipitation and subcellular co-localization by immunofluorescence










