| Host: |
Mouse |
| Applications: |
IP |
| Reactivity: |
Species independent |
| Note: |
STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS. |
| Short Description: |
Mouse monoclonal antibody anti-DDDDK-Tag is suitable for use in Immunoprecipitation research applications. |
| Clonality: |
Monoclonal |
| Clone ID: |
S5767MM |
| Conjugation: |
Magnetic Beads |
| Isotype: |
IgG1 |
| Formulation: |
PBS with 0.05% Proclin300, pH7.3. |
| Purification: |
Affinity purification |
| Dilution Range: |
IP 30ul antibody (bead slurry) for 200 Mu g-400 Mu g extracts of whole cells |
| Storage Instruction: |
Store at 4°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles. |
| Immunogen: |
A synthetic peptide corresponding to DDDDK tag. |
| Immunogen Sequence: |
DYKDDDDK |
| 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. |
Information sourced from Uniprot.org
12 months for antibodies. 6 months for ELISA Kits. Please see website T&Cs for further guidance
