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> pCMV6-AN-mKate Mammalian Expression Vector

pCMV6-AN-mKate Mammalian Expression Vector

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Cat# PS100047

Size : 10ug

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pCMV6-AN-mKate Mammalian Expression Vector

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SKU
PS100047
pCMV6-AN-mKate, mammalian vector with N-terminal mKate, 10ug

Datasheet SDS Vector Sequence
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Size
Specifications
Product Data
N-Tag mKate
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Expression Promoter CMV
Features
  • ORFs cloned in this vector will be expressed in mammalian cells as a tagged protein with an N-terminal mKate2 tag.
  • mKate2 possesses fluorescence with excitation/emission maxima at 588 and 633 nm, mKate2 is almost 3-fold brighter than TagFP635 and is 10-fold brighter than mPlum at physiological pH 7.5. Within the optical window optimal for light penetration in living tissues, calculated brightness of mKate2 is at least 2-fold higher compared to any monomeric fluorescent protein reported to date.
    mKate2 is characterized by complete and fast chromophore maturation at 37°C with maturation half-time <20 min (versus 40 min for mCherry). It is more photostable under both widefield and confocal illumination than other monomeric far-red proteins, including TagFP635, mRaspberry and mPlum. The high brightness, far-red emission spectrum, excellent pH resistance and photostability, coupled with low toxicity demonstrated in transgenic Xenopus laevis embryos, make mKate2 a superior fluorescent tag for imaging in living tissues.
    mKate2 is mainly intended for protein labeling. Its far-red fluorescence allows easy and reliable separation from standard green fluorescent labels in dual-color high-throughput assays.
  • If the N-terminal tagging interferes with the protein’s function, you can choose the C-terminal mKate2-tagging vector, PS100039.
  • mKate_F Primer can be used to sequence the target sequence after cloning.
  • XL39_R Primer can be used to sequence the target sequence after cloning.
Download Vector Sequence
Schematic of the multiple cloning sites
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Product Manuals
FAQs
  • FAQ for Tagged Cloning Vectors
Vector Resources