Immunofluorscence  53BP1 [H-300] Rabbit Human

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Get tips on using Anti-UCP-1 antibody produced in rabbit to perform Immunohistochemistry Mouse - UCP1

Products Sigma-Aldrich Anti-UCP-1 antibody produced in rabbit

Get tips on using PCNA (D3H8P) XP® Rabbit mAb #13110 to perform Immunohistochemistry Mouse - PCNA

Products Cell Signaling Technology PCNA (D3H8P) XP® Rabbit mAb #13110

Get tips on using Cleaved Notch1 (Val1744) (D3B8) Rabbit mAb #4147 to perform Immunohistochemistry Mouse - Notch1

Products Cell Signaling Technology Cleaved Notch1 (Val1744) (D3B8) Rabbit mAb #4147

Get tips on using VEGF Receptor 2 (55B11) Rabbit mAb #2479 to perform Western blotting VEGF

Products Cell Signaling Technology VEGF Receptor 2 (55B11) Rabbit mAb #2479

Get tips on using p21 Waf1/Cip1 (12D1) Rabbit mAb #2947 to perform Western blotting p21

Products Cell Signaling Technology p21 Waf1/Cip1 (12D1) Rabbit mAb #2947

Human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs) have been greatly used for studies on embryonic development and cell differentiation.iPSCs provide a stable source for either self-renewal or differentiation into suitable cells when cultured in a particular environment. Pluripotent cell culture was originally started by deriving cells from inner cell mass (ICM) from pre-implanted blastocysts, these were called embryonic stem cells. These cells after isolation can be grown on traditional extracellular matrices (like mouse embryonic fibroblasts, MEFs) or feeder-free culture systems. DMEM/F12 has been the most commonly used basal media in the culture of pluripotent cells. These cells are cultured at normal atmospheric oxygen levels, 21%, however, some studies have proposed that 4% oxygen tension may be better for hESC growth. Higher D-glucose concentration (4.2g/l) and osmolarity (320mOsm) that mimics the natural environment of embryonic tissue are optimal for the growth of hESCs. Supplements like N2 and/or B-27, in the presence of growth factors like bFGF, have been shown to increase pluripotency of these cells. bFGF, FGF2 and other ligands of receptor tyrosine kinases like IGF are also required or maintain self-renewal ability of these cells. TGF𝛃1, by its activation of SMAD2/3 signalling, also represses differentiation of iPSCs. Other compounds like ROCK inhibitors reduce blebbing and apoptosis in these cells to maintain their clonogenicity. However, an inhibitor for LIF (leukaemia inhibitory factor, which is one of the pluripotent genes) has an opposing effect. Therefore, it is important to understand the culture conditions and media composition that affect downstream signalling in hESCs or iPSCs that may lead to their differentiation.

Cell culture media Stem cell culture media h-medial pallium induction and culture

Get tips on using ICAM-1 Recombinant Rabbit Monoclonal Antibody (9H21L19) to perform Western blotting ICAM-1

Products Thermo Fisher Scientific ICAM-1 Recombinant Rabbit Monoclonal Antibody (9H21L19)

Get tips on using Cyclin D1 Recombinant Rabbit Monoclonal Antibody (SP4) to perform Western blotting Cyclin D1

Products Thermo Fisher Scientific Cyclin D1 Recombinant Rabbit Monoclonal Antibody (SP4)

Get tips on using Anti-β2-Microglobulin antibody produced in rabbit to perform Western blotting β₂ microglobulin

Products Sigma-Aldrich Anti-β2-Microglobulin antibody produced in rabbit

Get tips on using Anti-AP-1 antibody produced in rabbit to perform Western blotting C-Jun

Products Merck Millipore Anti-AP-1 antibody produced in rabbit

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