SKU: WP6434 Categories: ,

TRIM9 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP6434-100
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Product details

Background:

Specifications

Size50μL/100μL
TargetTRIM9
ReactivityHuman, Mouse, Rat
ApplicationsWB
MW(Calculated)78kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
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 TRIM9
SpecificityThis antibody detects endogenous levels of TRIM9 at Human, Mouse,Rat
Gene NameTRIM9 KIAA0282 RNF91
Protein NameE3 ubiquitin-protein ligase TRIM9 (RING finger protein 91) (Tripartite motif-containing protein 9)
Other Name
SpeciesHuman
Gene ID114088
UniprotQ9C026,
Species.1Mouse
Gene ID.194090
Uniprot.1Q8C7M3,
Species.2Rat
Gene ID.2155812
Uniprot.2Q91ZY8
Cellular LocalizationCytoplasm . Cell projection, dendrite . Cytoplasmic vesicle, secretory vesicle, synaptic vesicle . Cell junction, synapse . Cytoplasm, cytoskeleton . Enriched at synaptic terminals where it exists in a soluble form and a synaptic vesicle-associated form. Associated with the cytoskeleton (By similarity). Found in proximal dendrites of pyramidal neurons in the cerebral cortex and hippocampus, and Purkinje cells in the cerebellum (PubMed:20085810). .
Tissue ExpressionBrain. Highly expressed in the cerebral cortex (at protein level). Severely decreased in the affected brain areas in Parkinson disease and dementia with Lewy bodies.
Signaling_pathway
Research Areas
FunctionE3 ubiquitin-protein ligase which ubiquitinates itself in cooperation with an E2 enzyme UBE2D2/UBC4 and serves as a targeting signal for proteasomal degradation. May play a role in regulation of neuronal functions and may also participate in the formation or breakdown of abnormal inclusions in neurodegenerative disorders. May act as a regulator of synaptic vesicle exocytosis by controlling the availability of SNAP25 for the SNARE complex formation.
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