pCMV6-AC-RFP
PrecisionShuttle™ mammalian expression vector for fusing an ORF to a C-terminal TurboRFP tag.
Sequence Author: OriGene
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Sticky ends from different AlwNI sites may not be compatible. |
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PciI is inhibited by nonionic detergents. |
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Sticky ends from different BsmI sites may not be compatible. |
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Sticky ends from different PfoI sites may not be compatible. |
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The 1-base overhangs produced by PflFI may be hard to ligate.Sticky ends from different PflFI sites may not be compatible. |
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The 1-base overhangs produced by Tth111I may be hard to ligate.Sticky ends from different Tth111I sites may not be compatible. |
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Prolonged incubation with NdeI may lead to removal of additional nucleotides. |
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After cleavage, BamHI-HF® (but not the original BamHI) can remain bound to DNA and alter its electrophoretic mobility. |
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Efficient cleavage requires at least two copies of the SgrAI recognition sequence. |
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Efficient cleavage requires at least two copies of the RsrII recognition sequence. Sticky ends from different RsrII sites may not be compatible.For full activity, add fresh DTT. |
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BsiWI is typically used at 55°C, but is 50% active at 37°C. |
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PaeR7I does not recognize the sequence CTCTCGAG. |
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Sticky ends from different PasI sites may not be compatible. |
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Sticky ends from different Bsu36I sites may not be compatible. |
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PshAI quickly loses activity at 37°C, but can be used at 25°C for long incubations. |
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FseI gradually loses activity when stored at -20°C. |
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Efficient cleavage requires at least two copies of the SacII recognition sequence. |
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Sticky ends from different EcoO109I sites may not be compatible. |
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Cleavage may be enhanced when more than one copy of the Bpu10I recognition sequence is present. This recognition sequence is asymmetric, so ligating sticky ends generated by Bpu10I will not always regenerate a Bpu10I site.Sticky ends from different Bpu10I sites may not be compatible. |
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Sticky ends from different BlpI sites may not be compatible. |
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Sticky ends from different BsmBI sites may not be compatible.BsmBI-v2 is an improved version of BsmBI. |
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Sticky ends from different BstXI sites may not be compatible. |
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The 1-base overhangs produced by XcmI may be hard to ligate.Sticky ends from different XcmI sites may not be compatible. |
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* Blocked by Dcm methylation. Sticky ends from different SexAI sites may not be compatible. |
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* Blocked by Dam methylation. |
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Efficient cleavage requires at least two copies of the NarI recognition sequence. |
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Efficient cleavage requires at least two copies of the PluTI recognition sequence. |
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VP1.5 (forward primer) 18-mer / 44% GC 1 binding site 839 .. 856 = 18 annealed bases Tm = 51°C |
XL39 (reverse primer) 20-mer / 55% GC 1 binding site 1893 .. 1912 = 20 annealed bases Tm = 59°C |
AmpR 5173 .. 6033 = 861 bp 286 amino acids = 31.6 kDa 2 segments Segment 2: 5173 .. 5964 = 792 bp 263 amino acids = 28.9 kDa Product: β-lactamase confers resistance to ampicillin, carbenicillin, and related antibiotics |
AmpR 5173 .. 6033 = 861 bp 286 amino acids = 31.6 kDa 2 segments |