SKU: WP2649 Categories: ,

DPP6 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP2649-100
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Product details

Background:

This gene encodes a single-pass type II membrane protein that is a member of the peptidase S9B family of serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Variations in this gene may be associated with susceptibility to amyotrophic lateral sclerosis and with idiopathic ventricular fibrillation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014],

Specifications

Size50μL/100μL
TargetDPP6
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)95kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; ELISA 1:5000-20000
FormulationLiquid in PBS containing 50% glycerol,0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human protein . at AA range: 750-830
SpecificityDPP6 Polyclonal Antibody detects endogenous levels of protein.
Gene NameDPP6
Protein NameDipeptidyl aminopeptidase-like protein 6 (DPPX) (Dipeptidyl aminopeptidase-related protein) (Dipeptidyl peptidase 6) (Dipeptidyl peptidase IV-like protein) (Dipeptidyl peptidase VI) (DPP VI)
Other Name
SpeciesHuman
Gene ID1804
UniprotP42658,
Species.1Mouse
Gene ID.1
Uniprot.1Q9Z218,
Species.2Rat
Gene ID.2
Uniprot.2P46101
Cellular LocalizationCell membrane; Single-pass type II membrane protein .
Tissue ExpressionExpressed predominantly in brain.
Signaling_pathway
Research Areas
FunctionDisease:Genetic variation in DPP6 may influence susceptibility to amyotrophic lateral sclerosis (ALS). ALS is a severely disabling and lethal disorder caused by progressive degeneration of motor neurons in the brain, spinal cord and brainstem.,Function:May be involved in the physiological processes of brain function. Has no dipeptidyl aminopeptidase activity. May modulate the cell surface expression and the activity of the potassium channel KCND2.,similarity:Belongs to the peptidase S9B family.,subunit:Homodimer. Binds KCND2.,tissue specificity:Expressed predominantly in brain.,
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