HRP-conjugated Rabbit anti DDDDK-Tag mAb- ABclonal,ABclonal,AE095

Reactivity

Species independent

Application

WB, ELISA

Conjugate

HRP

Platform ID

BAB650944392

ABclonal

Headquarters

500W Cummings Park, Ste. 6500 Woburn, MA 01801

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Product Specifications
Scientific Background

Specifications

NameHRP-conjugated Rabbit anti DDDDK-Tag mAb- ABclonal
Cat. No.AE095
RRID#N/A
IsotypeIgG
ReactivitySpecies independent
ConjugationHRP
ApplicationWB, ELISA
Working DilutionsWB:1:2000-6000 | ELISA:Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Clone NumberARC5111-01-HRP
Molecular Weight50kDa/46kDa
ImmunogenSynthetic peptide. This information is considered to be commercially sensitive.
PurityAffinity purification
Appearance/FormLiquid
StorageStore at -20℃. Avoid freeze / thaw cycles.; Buffer: PBS containing 50% glycerol and 0.2% BSA, preserved with proclin300 or sodium azide (as specified on the Certificate of Analysis), pH 7.3
Regulatory StatusResearch Use Only

Scientific Background

FLAG-tag, or FLAG octapeptide, or FLAG epitope, is a polypeptide protein tag that can be added to a protein using recombinant DNA technology, having the sequence motif DYKDDDDK. It has been used for studying proteins in living cells and for protein purification by affinity chromatography. It has been used to separate recombinant, overexpressed protein from wild-type protein expressed by the host organism. It can also be used in the isolation of protein complexes with multiple subunits, because its mild purification procedure tends not to disrupt such complexes. It has been used to obtain proteins of sufficient purity and quality to carry out 3D structure determination by x-ray crystallography.A FLAG-tag can be used in many different assays that require recognition by an antibody. If there is no antibody against a given protein, adding a FLAG-tag to a protein allows the protein to be studied with an antibody against the FLAG sequence. Examples are cellular localization studies by immunofluorescence or detection by SDS PAGE protein electrophoresis and Western blotting.

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