S-Tag (D2K2V) Rabbit Monoclonal Antibody (BSA and Azide Free)#80110,Cell Signaling Technology (CST),80110
S-Tag (D2K2V) Rabbit Monoclonal Antibody (BSA and Azide Free) recognizes transfected levels of recombinant protein containing an S-Tag.
Host
Rabbit
Reactivity
All Species Expected
Platform ID
BAB255943968
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Cell Signaling Technology (CST)
Contact
Tel: 877-616-2355,978-867-2388
Fax: 877-616-2355
Email:
Product Specifications
Scientific Background
Specifications
NameS-Tag (D2K2V) Rabbit Monoclonal Antibody (BSA and Azide Free)#80110
Cat. No.80110
HostRabbit
SensitivityTransfected Only
ReactivityAll Species Expected
ImmunogenIgG
FormulationThis product is the carrier free version of product #12774. All data were generated using the same antibody clone in the standard formulation which contains BSA and glycerol.This formulation is ideal for use with technologies requiring specialized or custom antibody labeling, including fluorophores, metals, lanthanides, and oligonucleotides. It is not recommended for ChIP, ChIP-seq, CUT&RUN or CUT&Tag assays. If you require a carrier free formulation for chromatin profiling, pleasecontact us. Optimal dilutions/concentrations should be determined by the end user.BSA and Azide Free antibodies are quality control tested by size exclusion chromatography (SEC) to determine antibody integrity.
StorageStore at -20°C.This product will freeze at -20°C so it is recommended to aliquot into single-use vials to avoid multiple freeze/thaw cycles.A slight precipitate may be present and can be dissolved by gently vortexing. This will not interfere with antibody performance.
Regulatory StatusResearch Use Only
Scientific Background
Epitope tags are useful for the labeling and detection of proteins using immunoblotting, immunoprecipitation, and immunostaining techniques. Because of their small size, they are unlikely to affect the tagged protein’s biochemical properties.S-Tag is an epitope tag composed of a 15 residue peptide that, together with S-protein, comprises pancreatic ribonuclease S (1).Raines, R.T. et al. (2000)Methods Enzymol326, 362-76.
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