MAB4419
Anti-OCT-4 [POU5F1] Antibody, clone 7F9.2
clone 7F9.2, from mouse
Synonym(s):
Octamer-binding transcription factor 3, POU class 5 homeobox 1, POU domain class 5, transcription factor 1, POU-type homeodomain-containing DNA-binding protein, octamer-binding transcription factor-3
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About This Item
biological source
mouse
Quality Level
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
7F9.2, monoclonal
species reactivity
human, mouse
technique(s)
flow cytometry: suitable
immunocytochemistry: suitable
western blot: suitable
input
sample type: human embryonic stem cell(s)
sample type induced pluripotent stem cell(s)
sample type: mouse embryonic stem cell(s)
isotype
IgG1κ
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Gene Information
human ... POU5F1(5460)
mouse ... Pou5F1(18999)
Related Categories
General description
Immunogen
Application
Stem Cell Research
Pluripotent & Early Differentiation
Flow Cytometry: Recommended working dilution is 2 µg/mL.
Immunocytochemistry: Recommended working dilution is 1:100 – 1: 200.
Biochem/physiol Actions
Physical form
Preparation Note
Other Notes
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Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
Skip weekend feedings. Defined serum-free and feeder-free expansion media for human pluripotent stem cells (ES and iPS cells). See publications and protocols.
The Simplicon™ RNA Reprogramming Technology is a next generation reprogramming system that uses a single synthetic, polycistronic self-replicating RNA strand engineered to mimic cellular RNA to generate human iPS cells.
Human iPSC neural differentiation media and protocols used to generate neural stem cells, neurons and glial cell types.
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As the focus of stem cell research undergoes a transition from animal to human models, researchers are in critical need of validated products to support the isolation, maintenance, differentiation, and characterization of human stem cells. While many reagents designed for rodent systems can be applied to human stem cell studies, they are not truly optimized for robust human stem cell culture or analysis. This is why human stem cell researchers have always trusted EMD Millipore, the first provider of commercially available human embryonic stem cells and human neural stem cell lines, to accelerate their research. All of our human stem cell systems are extensively tested in defined media culture, and differentiated progeny are comprehensively characterized with highly validated antibodies and detection reagents.
Traditionally, culture and expansion of mouse embryonic stem cells (mESC) is performed using several single-layer T-flasks or Petri dishes. Harvesting and analyzing stem cells from multiple culture vessels is a repetitive and time-intensive process that consumes valuable incubator space. Here, we report a method for expanding mESCs using a new multilayer cell culture flask. The Millicell HY multilayer culture flask makes expansion and harvesting of mESCs faster and easier than traditional culture methods. The method for using the new flasks is linearly scalable per unit surface area. Therefore, no reoptimization of procedure is required – culture conditions and media volume are identical, regardless of whether culture is performed in traditional single-layer devices or in a Millicell HY culture flask. Resulting morphology, cell recovery, viability, and pluripotency of mESCs were not significantly different between multilayer flask culture and single-layer flask culture methods.
Millipore’s new STEMCCA lentivirus reprogramming kits make it easier than ever to generate induced pluripotent stem (iPS) cells. Unlike traditional iPS generation which requires simultaneous co-infection by four separate expression vectors, the STEMCCA kits use a single polycistronic lentiviral vector to improve efficiency and reduce the number of viral integrations. The STEMCCA vector is comprised of the transcription factors Oct-4, Klf4, SOX-2, and c-Myc (OKSM), separated by the self-cleaving 2A peptide and IRES sequences 1,2. It is also available with flanking LoxP sites incorporated for Cre-mediated excision of the exogenous reprogramming transgenes. STEMCCA Vector Advantages: (1) Efficient: uses a single vector with four transcription factors rather than co-transducing four separate expression vectors (2) Minimizes viral integrations: single vector reduces the risks of insertional mutagenesis and viral reactivation and (3) Excisable: Cre/LoxP-regulated version enables removal of reprogramming transgenes.
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