AffiAB® Anti-PREPL Antibody [JE65-64]
The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene. Serine peptidase whose precise substrate specificity remains unclear. Does not cleave peptides after a arginine or lysine residue. Regulates trans-Golgi network morphology and sorting by regulating the membrane binding of the AP-1 complex. May play a role in the regulation of synaptic vesicle exocytosis.
Antibody type
Recombinant Rabbit monoclonal Antibody
Uniprot ID
SwissProt: Q4J6C6 Human; SwissProt: Q8C167 Mouse; SwissProt: Q5HZA6 Rat
Recombinant
YES
Conjugation
Non-conjugated
Host
Rabbit
Isotype
IgG
Clone
JE65-64
KO/KD
N/A
Species reactivity
Human, Mouse, Rat
Tested applications
WB, IHC-P
Predicted species reactivity
N/A
Immunogen
Recombinant protein within human PREPL aa 621-720/727.
Storage
Store at +4°C after thawing. Aliquot store at -20°C. Avoid repeated freeze / thaw cycles.
Form
Liquid
Storage buffer
1*TBS (pH7.4) , 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration
1 mg/mL.
Purity
Protein A affinity purified.
Signal pathway
N/A
Recommended dilutions
WB: 1:500
; IHC-P: 1:400
Molecular Weight
Predicted band size: 84 kDa
Subcellular location
Cytoskeleton, Nucleus, cytosol, trans-Golgi network, Golgi apparatus.
Positive control
NIH/3T3 cell lysates, PC-12 cell lysates, rat hippocampus tissue, rat brain tissue, mouse hippocampus tissue, mouse brain tissue.