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SCR508

Sigma-Aldrich

TAT-CRE Recombinase

TAT-CRE Recombinase is a recombinant cell-permeant fusion cre-recombinase protein consisting of TAT sequence, a nuclear localization sequence (NLS) and it is known to catalyze the site specific recombination event between two loxP DNA sites.

Synonim(y):

Integrase, Recombinase Cre, cre recombinase

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Wybierz wielkość

1500 UNITS
2770,00 zł

2770,00 zł


Przewidywany termin wysyłki01 kwietnia 2025Szczegóły



Wybierz wielkość

Zmień widok
1500 UNITS
2770,00 zł

About This Item

Kod UNSPSC:
12352204
eCl@ss:
32160405
NACRES:
NA.75

2770,00 zł


Przewidywany termin wysyłki01 kwietnia 2025Szczegóły


pochodzenie biologiczne

Escherichia coli

Poziom jakości

rekombinowane

expressed in E. coli

Próba

>70% (SDS-PAGE)

Formularz

liquid

metody

cell culture | stem cell: suitable

Warunki transportu

dry ice

Opis ogólny

Cre Recombinase is an enzyme from bacteriophage P1 that catalyzes the site-specific recombination between two DNA recognition sites termed loxP sites. The LoxP recognition site consists of two 13 bp inverted repeats flanking a 8 bp spacer region. Because the Cre gene and loxP sites are not native to the genomes of most species, LoxP sites can be engineered and introduced into target cells and thus used as a means to precisely control the expression of genes in vitro (i.e. cultured cells) and in vivo (i.e. animal models).

• If LoxP sites are located on different chromosomes, Cre recombinase will mediate a chromosomal translocation.
• If LoxP sites are oriented in the opposite direction, Cre recombinase will mediate an inversion of the floxed segment.
• If LoxP sites are oriented in the same direction, Cre recombinase will mediate a deletion of the floxed segment.

In this way, placement of the LoxP sites allows genes to be activated, repressed or exchanged for other genes.

EMD Millipore’s TAT-CRE Recombinase is a recombinant cell-permeant fusion protein consisting of a basic protein translocation peptide derived from HIV-TAT (TAT), a nuclear localization sequence (NLS), the Cre protein and an N-terminal histidine tag (H6) for efficient purification of the protein from E. coli.

EMD Millipore’s TAT-CRE Recombinase has been shown to effectively excise STEMCCA viral transgenes from both Human and Mouse IPS cells.

Zastosowanie

EMD Millipore has developed a cell-permeant TAT-CRE Recombinase fusion protein which can be directly delivered to mammalian cells and results in high recombination efficiencies (75 – 100% in mouse and ~ 60% in human cells). TAT-CRE readily translocates to mammalian cells and can catalyze highly efficient recombination. The dose and timing of Cre exposure can be precisely controlled thus allowing for the careful titration of Cre activity.

Jakość

Each lot of TAT-CRE Recombinase protein is rigorously quality control tested for the following parameters:

  • Purity: single band around 41 kDa with greater than 70% protein purity on an SDS-PAGE gel
  • Functional activity: mediates recombination of LoxP-modified alleles in a HEK293T- Cre reporter cell line
  • Endotoxin levels: less than 1 EU/ug protein

Definicja jednostki

A standard of 100 Units is defined as the amount of TAT-CRE (ug) in 1.0 mL of tissue culture medium that is required to induce 50% GFP expression in a HEK293T loxp reporter cell line assay.

Postać fizyczna

Recombinant protein is supplied in buffer containing 50% glycerol (v/v) 500 mM NaCl and 20 mM HEPES at pH 7.4

Przechowywanie i stabilność

Stable for 3 months from date of receipt when stored at -20°C or -80°C. Upon first thaw, centrifuge the vial and gently mix the solution. Aliquot into smaller working volumes and freeze at -20°C or -80°C. Before use, dilute TAT-CRE to the appropriate concentration with culture medium and filter through a 0.2um low protein binding syringe filter (Millipore Cat. No. SLGV 033RS or SLGV013 SL).
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Kod klasy składowania

10 - Combustible liquids

Klasa zagrożenia wodnego (WGK)

WGK 1


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Stem cell engineering using transducible Cre recombinase.
Nolden, Lars, et al.
Methods in Molecular Medicine, 140, 17-32 (2007)
Mian Zhang et al.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 34(4), 726-738 (2018-11-30)
Traumatic joint injuries produce osteoarthritic cartilage manifesting accelerated chondrocyte terminal differentiation and matrix degradation via unknown cellular and molecular mechanisms. Here we report the ability of biomechanical stress to increase expression of the calcium-sensing receptor (CaSR), a pivotal driver of
Stage-specific conditional mutagenesis in mouse embryonic stem cell-derived neural cells and postmitotic neurons by direct delivery of biologically active Cre recombinase.
Haupt, Simone, et al.
Stem Cells, 25, 181-188 (2007)
Ramdane Igalouzene et al.
The Journal of clinical investigation, 132(8) (2022-04-16)
SMAD4, a mediator of TGF-β signaling, plays an important role in T cells to prevent inflammatory bowel disease (IBD). However, the precise mechanisms underlying this control remain elusive. Using both genetic and epigenetic approaches, we revealed an unexpected mechanism by
Egor Dzyubenko et al.
Frontiers in cellular neuroscience, 15, 689268-689268 (2021-07-03)
Astrocytic networks are critically involved in regulating the activity of neuronal networks. However, a comprehensive and ready-to-use data analysis tool for investigating functional interactions between the astrocytes is missing. We developed the novel software package named "Astral" to analyse intercellular

Produkty

Fibroblast growth factors (FGFs) regulate developmental pathways and mesoderm/ectoderm patterning in early embryonic development.

Czynniki wzrostu fibroblastów (FGF) regulują szlaki rozwojowe i kształtowanie mezodermy/ektodermy we wczesnym rozwoju embrionalnym.

Protokoły

Stem cell reprogramming protocols to generate human induced pluripotent stem cells (iPSCs) including viral and non-viral RNA based methods.

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