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OTUD1 Rabbit Polyclonal Antibody

Catalog Number: orb587697

DispatchUsually dispatched within 3-7 working days
$ 600.00
Catalog Numberorb587697
CategoryAntibodies
DescriptionRabbit polyclonal antibody to OTUD1
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsWB
Predicted ReactivityBovine, Canine, Equine, Mouse, Rat
ReactivityHuman
ImmunogenThe immunogen is a synthetic peptide directed towards the C-terminal region of Human OTUD1
Concentration0.5 mg/ml
Form/AppearanceLiquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
ConjugationUnconjugated
MW51 kDa
TargetOTUD1
UniProt IDQ5VV17
Protein SequenceSynthetic peptide located within the following region: NGHYDAVFDHSYPNPEYDNWCKQTQVQRKRDEELAKSMAISLSKMYIEQN
NCBINP_001138845
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Buffer/PreservativesLiquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Alternative namesDUBA7, OTDC1
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NoteFor research use only
Expiration Date12 months from date of receipt.
OTUD1 Rabbit Polyclonal Antibody

25 ug of the indicated Human whole cell extracts was loaded onto a 12% SDS-PAGE gel. 1 ug/ml of the antibody was used in this experiment.

OTUD1 Rabbit Polyclonal Antibody

Sample Type: HepG2 Whole Cell lysates, Antibody Dilution: 1.0 ug/ml.

OTUD1 Rabbit Polyclonal Antibody

Positive control (+): Human lung (LU), Negative control (-): Human brain (BR), Antibody concentration: 1 ug/ml.

OTUD1 Rabbit Polyclonal Antibody

Surface Plasmon Resonance Kinetic Characterization of Polyclonal Antibody Affinity. Purified polyclonal antibodies were immobilized on a Protein A/G coated Carterra LSA sensor chip (PAGH200M) at concentrations of 5, and 50 ug/ml in duplicate. Antibodies on the surface were exposed to interaction with peptides sequentially via microfluidic controlled flow at 333nM peptide concentration for kinetic characterization of the binders for affinity and specificity, followed by curve fitting using the Kinetics software. Kd determinations for both concentrations were averaged and results and standard deviation are shown.

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