pCLIPfVector from New England Biolabs

Product Specs
ItempCLIPfVector
CompanyNew England Biolabs
Price $183.00 Inquire
Catalog NumberN9215S
Quantity20 µg
Vector NamepCLIPfVector
ApplicationsCellular Biology
TypeVector
Nucleic Acid TypeExpression Vectors
Expression System (standardized)Mammalian
Conjugate/Tag/Label (standardized)Other non-fluorescent conjugates
Selectable Marker (standardized)Neomycin
Temperature-20 C

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New England Biolabs

240 County Road

Ipswich, Massachusetts 1938

United States

Phone: 800-632-5227
800-632-7799
978-921-1350

Company Profile

Website: http://www.neb.com

(1) Newly synthesized claudins but not occludin are added to the basal side of the tight junctionMolecular biology of the cellJune 1, 2019Van Itallie CM, Lidman KF, Tietgens AJ, Anderson JM.2001) as a template and cloning into the BamHI/XhoI sites in pSNAPf and pCLIPf (New England Biolabs, N9215S). Sequences of all primers are shown in Supplemental Table 1. SNAP ocln construct was made by PCR from

(2) Bright multicolor labeling of neuronal circuits with fluorescent proteins and chemical tagsElifeNovember 20, 2018Richi Sakaguchi, Marcus N Leiwe, Takeshi ImaiAdvanced vector (Clontech). SNAPf and CLIPf tag genes were obtained from New England Biolabs (#N9183S, #N9215S), and the HaloTag gene was obtained from Promega (#G3780). AAV2-Tetbow vectors were generated by modifying

(3) Bright multicolor labeling of neuronal circuits with fluorescent proteins and chemical tagseLifeNovember 20, 2018Richi Sakaguchi, Marcus N Leiwe, Takeshi ImaiAdvanced vector (Clontech). SNAPf and CLIPf tag genes were obtained from New England Biolabs (#N9183S, #N9215S), and the HaloTag gene was obtained from Promega (#G3780). AAV2-Tetbow vectors were generated by modifying

(4) Quantifying transcription factor binding dynamics at the single-molecule level in live cellsMethodsJuly 1, 2017Diego M. Presman, David A. Ball, Ville Paakinaho, Jonathan B. Grimm, Luke D. Lavis, Tatiana S. Karpova, Gordon L. HagerCMV promoter. This was generated by PCR amplification from HaloTag–GR and sub cloned into the pCLIPf (N9215S, New England Biolabs) backbone with NheI and AgeI sites. The mEOS3–GR was generated by purification

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pCLIPfVector

pCLIPfVector from New England Biolabs

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pCLIPfVector from New England Biolabs

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