Renin receptor,ATP6AP2 antibody

Synonyms:APT6M8 9 antibody, ATP6AP2 antibody, ATP6IP2 antibody, ATP6M8 9 antibody, CAPER antibody, ELDF10 antibody, HT028 antibody, M8 9 antibody, MRXE antibody, MSTP009 antibody, N14F antibody, PRR antibody, PSEC0072 antibody, Renin receptor antibody, RENIN RECEPTOR antibody, ATP6AP2 antibody, Renin/prorenin receptor antibody, V ATPase M8.9 subunit antibody, XMRE antibody
Catalogue No.:FNab07241Reactivity:Human, Mouse, Rat
Host:RabbitTested Application:ELISA, WB, IHC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
Renin receptor,ATP6AP2 antibody
Catalogue No.
FNab07241
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
ATPase, H+ transporting, lysosomal accessory protein 2
Alternative Names
APT6M8 9 antibody, ATP6AP2 antibody, ATP6IP2 antibody, ATP6M8 9 antibody, CAPER antibody, ELDF10 antibody, HT028 antibody, M8 9 antibody, MRXE antibody, MSTP009 antibody, N14F antibody, PRR antibody, PSEC0072 antibody, Renin receptor antibody, RENIN RECEPTOR antibody, ATP6AP2 antibody, Renin/prorenin receptor antibody, V ATPase M8.9 subunit antibody, XMRE antibody
UniProt ID
O75787
Observed MW
47kd
Application
Tested Applications
ELISA, WB, IHC
Recommended dilution
WB: 1:500-1:1000; IHC: 1:20-1:200
Validated Images
mouse eye tissue were subjected to SDS PAGE followed by western blot with FNab07241(ATP6AP2 antibody) at dilution of 1:600
Immunohistochemistry of paraffin-embedded human heart tissue slide using FNab07241(ATP6AP2 Antibody) at dilution of 1:50
Background
ATP6AP2, also named as ATP6IP2, CAPER, ELDF10, N14F, ATP6M8-9, Renin receptor and prorenin receptor, is believed to potentiate the renin–angiotensin system(RAS), conferring to prorenin, a likely pathological role at tissue level. The PRR has been identified in the microvascular endothelial cells of the retina, in which it seems to be involved in pathological neovascularization processes. The present study demonstrates for the first time that the PRR is expressed in human ATP6AP2 and suggests a molecular mechanism by which hypertension may exacerbate the pathology of dry AMD.