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TC-FlAsH™ TC-ReAsH™ II In-Cell Tetracysteine Tag Detection Kit, with Mammalian TC-Tag Gateway™ Expression Vectors (Green Fluorescence) (Red Fluorescence)
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Invitrogen™

TC-FlAsH™ TC-ReAsH™ II In-Cell Tetracysteine Tag Detection Kit, with Mammalian TC-Tag Gateway™ Expression Vectors (Green Fluorescence) (Red Fluorescence)

TC-FlAsH™ TC-ReAsH™ II In-Cell Tetracysteine Tag Detection Kit is an expression tag-based fluorescence labeling system for live-cell labeling. The expressionRead more
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Catalog NumberQuantity
T345631 Kit
Catalog number T34563
Price (USD)
2,880.00
1 kit
Estimated availability date 12-Aug-2025
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Quantity:
1 Kit
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Price (USD)
2,880.00
1 kit
Add to cart
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TC-FlAsH™ TC-ReAsH™ II In-Cell Tetracysteine Tag Detection Kit is an expression tag-based fluorescence labeling system for live-cell labeling. The expression construct is created when the Gateway entry clone (containing the gene of interest) is recombined with one of two destination vectors (pcDNA6.2/nTC-Tag-DEST for N-terminal tagging or pcDNA6.2/cTC-Tag-DEST for C-terminal tagging). The expression construct is then used to transform the host strain. The protein can be detected either with green-fluorescent FlAsH-EDT2 reagent or red-fluorescent ReAsH-EDT2 reagent. The tag is very small (6 amino acids) and the protein of interest is fluorescent only when the labeling reagent is added. BAL wash buffer replaces the previously supplied Disperse Blue 3 and EDT-based wash buffer as an olfactorily more agreeable reagent that yields superior signal to noise.

The kit contains FlAsH-EDT2 labeling reagent, ReAsH-EDT2 labeling reagent, BAL wash buffer, pcDNA6.2/cTC-Tag-DEST, pcDNA6.2/nTC-Tag-DEST, and pcDNA6.2/nTC-Tag-p64 Control Plasmid. BAL wash buffer should be stored at 4°C, and the rest of the kit stored at -20°C, protected from light. The kit is stable for 6 months when stored correctly.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
AssayTetracysteine Tag Detection
ColorRed, Green
Detection MethodFluorescence
For Use With (Equipment)Fluorescence Microscope
Label or DyeFlAsH, ReAsH
Product LineGateway, TC-FlAsH II, TC-ReAsH II
Product TypeTetracysteine Tag Detection Kit
Quantity1 Kit
Shipping ConditionWet Ice
FormatKit
Unit Size1 kit
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
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Figures

Fluorescence spectra

Fluorescence spectra

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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3008215Certificate of AnalysisSep 03, 2024T34563
2826930Certificate of AnalysisNov 06, 2023T34563
2770777Certificate of AnalysisSep 28, 2023T34563
2539053Certificate of AnalysisFeb 16, 2023T34563
2507856Certificate of AnalysisJul 19, 2022T34563
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Safety Data Sheets

Vector Information

Vector Name
Vector Map
Polylinker
Sequence
Restriction
pZErO-1.1 (replaced with pZErO-1)
pYesTrp2-RalGDS
pZeoSV (replaced with pZeoSV2)

Citations & References (16)

Citations & References
Abstract
Resolution of de novo HIV production and trafficking in immature dendritic cells.
Authors:Turville SG, Aravantinou M, Stössel H, Romani N, Robbiani M,
Journal:Nat Methods
PubMed ID:18059278
'The challenge in observing de novo virus production in human immunodeficiency virus (HIV)-infected dendritic cells (DCs) is the lack of resolution between cytosolic immature and endocytic mature HIV gag protein. To track HIV production, we developed an infectious HIV construct bearing a diothiol-resistant tetracysteine motif (dTCM) at the C terminus ... More
Dynamic fluorescent imaging of human immunodeficiency virus type 1 gag in live cells by biarsenical labeling.
Authors:Rudner L, Nydegger S, Coren LV, Nagashima K, Thali M, Ott DE,
Journal:J Virol
PubMed ID:15767407
'Human immunodeficiency virus type 1 (HIV-1) Gag is the primary structural protein of the virus and is sufficient for particle formation. We utilized the recently developed biarsenical-labeling method to dynamically observe HIV-1 Gag within live cells by adding a tetracysteine tag (C-C-P-G-C-C) to the C terminus of Gag in both ... More
Fluorescence imaging of amyloid formation in living cells by a functional, tetracysteine-tagged alpha-synuclein.
Authors:Roberti MJ, Bertoncini CW, Klement R, Jares-Erijman EA, Jovin TM
Journal:Nat Methods
PubMed ID:17351621
'Alpha-synuclein is a major component of intraneuronal protein aggregates constituting a distinctive feature of Parkinson disease. To date, fluorescence imaging of dynamic processes leading to such amyloid deposits in living cells has not been feasible. To address this need, we generated a recombinant alpha-synuclein (alpha-synuclein-C4) bearing a tetracysteine target for ... More
Short tetracysteine tags to beta-tubulin demonstrate the significance of small labels for live cell imaging.
Authors:Andresen M, Schmitz-Salue R, Jakobs S
Journal:Mol Biol Cell
PubMed ID:15469986
'Genetically encoded tags are of fundamental importance for live cell imaging. We show that small tetracysteine (TetCys) tags can be highly advantageous for the functionality of the host protein compared with large fluorescent protein tags. One to three concatenated small TetCys tags as well as the large green fluorescent protein ... More
Specific covalent labeling of recombinant protein molecules inside live cells.
Authors:Griffin BA, Adams SR, Tsien RY,
Journal:Science
PubMed ID:9657724
'Recombinant proteins containing four cysteines at the i, i + 1, i + 4, and i + 5 positions of an alpha helix were fluorescently labeled in living cells by extracellular administration of 4'',5''-bis(1,3, 2-dithioarsolan-2-yl)fluorescein. This designed small ligand is membrane-permeant and nonfluorescent until it binds with high affinity and ... More
16 total citations

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