ARG62342

anti-DDDDK tag antibody [FG4R]

anti-DDDDK tag antibody [FG4R] for Dot blot,ELISA,ICC/IF,Immunoprecipitation,In situ hybridization,Western blot and Other

Controls and Markers antibody; Tag Internal Control antibody
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Overview

Product Description Mouse Monoclonal antibody [FG4R] recognizes DDDDK tag (Equivalent to Sigma's anti-FLAG antibodies).
Tested Reactivity Other
Tested Application Dot, ELISA, ICC/IF, IP, ISH, WB
Specificity Recognizes the N-terminal, C-terminal or internal DYKDDDDK-tagged fusion proteins.
Host Mouse
Clonality Monoclonal
Clone FG4R
Isotype IgG1
Target Name DDDDK tag
Antigen Species Others
Immunogen DYKDDDDK (FLAG) synthetic peptide conjugated to KLH.
Conjugation Un-conjugated

Application Instructions

Application Suggestion
Tested Application Dilution
DotAssay-dependent
ELISAAssay-dependent
ICC/IF1:500 - 1:2000
IPAssay-dependent
ISHAssay-dependent
WB1:1000 - 1:5000
Application Note The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Protein A Purified
Purification Note Protein A affinity chromatography from mouse ascites fluid.
Buffer 10mM PBS (pH 7.2) and 0.05% Sodium azide.
Preservative 0.05% Sodium azide
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Gene Full Name DDDDK Epitope Tag
Background Epitope tags provide a method to localize gene products in a variety of cell types, study the topology of proteins and protein complexes, identify associated proteins, and characterize newly identified, low abundance or poorly immunogenic proteins when protein specific antibodies are not available. Tagging with xxxDDDDK may be done at the N-terminus, N-terminus preceded by a methionine residue, C-terminus, and in internal positions of the target protein. The small size of the epitope tag and its high hydrophilicity tend to decrease the possibility of interference with protein expression, proteolytic maturation, antigenicity and function. The enterokinase cleavage site allows it to be completely removed from the purified fusion proteins.
Cleavage catalyzed by Cu2+ ions of the C-terminal xxxDDDDK from a fusion protein has been reported (Humphreys, D.P., et al., 1999). A sequence motif with five out of eight amino acid residues identical to the xxxDDDDK is found in both rat and mouse Mg2+ dependent protein b-phosphatase, as well as in the human and bovine enzyme.
Highlight Related products:
DDDDK antibodies; DDDDK Duos / Panels; Anti-Mouse IgG secondary antibodies;
Research Area Controls and Markers antibody; Tag Internal Control antibody

Customer's Feedback

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Review for anti-DDDDK tag antibody [FG4R]

Application:WB

Sample:293T and 293T+flag+mCherry

Sample Loading Amount:20 µg

Primary Antibody Dilution Factor:1:1000

Primary Antibody Incubation Time:overnight

Primary Antibody Incubation Temperature:4 ºC

Specific References

Quercetin Attenuates the Production of Pro-Inflammatory Cytokines in H292 Human Lung Epithelial Cells Infected with Pseudomonas aeruginosa, by Modulating ExoS Production

ELISA, WB / Other

Hye In Ahn et al.
J Microbiol Biotechnol.,  (2023)

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SCUBE3 downregulation modulates hepatocellular carcinoma by inhibiting CCNE1 via TGFβ/PI3K/AKT/GSK3β pathway

WB / 

Pan Xu et al.
Cancer Cell Int .,  (2022)

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The Functional Study of KEAP1 Gene and Its Mutation in NSCLC Cell Line:A Preliminary Experimental Study

Li Yan et al.
Progress in Modern Biomedicine,  (2021)

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Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.

WB, ICC/IF / Other

Bojian Li et al.
Mol Genet Genomic Med.,  (2021)

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Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect.

WB / Other

Wei Wei et al.
Clin Genet.,  (2020)

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