pE2-Crimson-C1 Vector

pE2-Crimson-C1 Vector

Brand: Takara Bio.
In stock
SKU
pE2-Crimson-C1 Vector
Grouped product items
Product Name Size
pE2-Crimson-C1 Vector
SKU: 632555
20 ug
Make An Enquiry
× Product Enquiry
pE2-Crimson-C1 Vector
pE2-Crimson-C1 Vector

Fill in the details below:

pE2-Crimson-C1 is a mammalian expression vector designed to express a protein of interest fused to the C-terminus of E2-Crimson, our brightest and fastest-maturing far-red Living Colors fluorescent protein. E2-Crimson was derived from DsRed-Express2, and retains its fast maturation, high photostability, increased solubility, and low cytotoxicity. The unmodified vector can be used to express E2-Crimson in mammalian cells. If required, stable transfectants can be selected using G418.

Overview

  • Far-red fluorescent protein
  • E2-Crimson fluorescent protein excitation and emission maxima: 611 and 646 nm, respectively
  • Several of our red fluorescent protein antibodies strongly detect E2-Crimson

Applications

  • Applications involving sensitive cells, such as primary cells and stem cells
  • Fusions
  • Protein localization studies
  • General reporter for mammalian cells
  • Monitoring transfection efficiencies
  • In vivo imaging

Schematic for fluorescent fusion protein vectors

Schematic for fluorescent fusion protein vectors

Schematic for fluorescent fusion protein vectors. Panel A. N-terminal fluorescent protein (FP) vector. Panel B. C-terminal fluorescent protein vector.

E2-Crimson is useful for confocal and STED (stimulated emission depletion) microscopy

E2-Crimson is useful for confocal and STED (stimulated emission depletion) microscopy

E2-Crimson is useful for confocal and STED (stimulated emission depletion) microscopy. The mammalian ER was imaged by conventional confocal microscopy (left) or by STED microscopy (right) with 635 nm excitation and a STED wavelength of 760 nm. The scale bar is 1 μm.

Write Your Own Review
You're reviewing:pE2-Crimson-C1 Vector
Your Rating

pE2-Crimson-C1 is a mammalian expression vector designed to express a protein of interest fused to the C-terminus of E2-Crimson, our brightest and fastest-maturing far-red Living Colors fluorescent protein. E2-Crimson was derived from DsRed-Express2, and retains its fast maturation, high photostability, increased solubility, and low cytotoxicity. The unmodified vector can be used to express E2-Crimson in mammalian cells. If required, stable transfectants can be selected using G418.

Overview

  • Far-red fluorescent protein
  • E2-Crimson fluorescent protein excitation and emission maxima: 611 and 646 nm, respectively
  • Several of our red fluorescent protein antibodies strongly detect E2-Crimson

Applications

  • Applications involving sensitive cells, such as primary cells and stem cells
  • Fusions
  • Protein localization studies
  • General reporter for mammalian cells
  • Monitoring transfection efficiencies
  • In vivo imaging

Schematic for fluorescent fusion protein vectors

Schematic for fluorescent fusion protein vectors

Schematic for fluorescent fusion protein vectors. Panel A. N-terminal fluorescent protein (FP) vector. Panel B. C-terminal fluorescent protein vector.

E2-Crimson is useful for confocal and STED (stimulated emission depletion) microscopy

E2-Crimson is useful for confocal and STED (stimulated emission depletion) microscopy

E2-Crimson is useful for confocal and STED (stimulated emission depletion) microscopy. The mammalian ER was imaged by conventional confocal microscopy (left) or by STED microscopy (right) with 635 nm excitation and a STED wavelength of 760 nm. The scale bar is 1 μm.

Write Your Own Review
You're reviewing:pE2-Crimson-C1 Vector
Your Rating