Anti-ATP6AP2 Antibody


Reactivity: Human,Mouse
Applications: ELISA,WB,IHC
Conjugation: Various

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Rabbit Anti-ATP6AP2 Antibody (CSB-PA002384ESR2HU)


Alternative names:

ATPase H(+)-transporting lysosomal accessory protein 2 Antibody,ATPase H(+)-transporting lysosomal-interacting protein 2 Antibody,ER-localized type I transmembrane adaptor Antibody,Embryonic liver differentiation factor 10 Antibody,N14F Antibody,Renin/prorenin receptor Antibody,Vacuolar ATP synthase membrane sector-associated protein M8-9 Antibody,ATP6M8-9 Antibody,V-ATPase M8.9 subunit Antibody,ATP6AP2 Antibody,ATP6IP2 Antibody, CAPER Antibody, ELDF10 Antibody,HT028 Antibody, MSTP009 Antibody, PSEC0072 Antibody

More alternative names for the antibody
APT6M8 9 antibody|APT6M8-9 antibody|ATP6AP2 antibody|ATP6IP2 antibody|ATP6M8-9 antibody|ATPase H(+)-transporting lysosomal accessory protein 2 antibody|ATPase H(+)-transporting lysosomal-interacting protein 2 antibody|ATPase H+ transporting lysosomal accessory protein 2 antibody|ATPase H+ transporting lysosomal interacting protein 2 antibody|ATPase H+ transporting lysosomal vacuolar proton pump membrane sector associated protein M8 9 antibody|ATPase membrane sector associated protein M8 9 antibody|ATPase, H+ transporting, lysosomal (vacuolar proton pump) membrane sector associated protein M8 9 antibody|CAPER antibody|ELDF10 antibody|Embryonic liver differentiation factor 10 antibody|ER localized type I transmembrane adaptor antibody|ER-localized type I transmembrane adaptor antibody|HT028 antibody|M8 9 antibody|M8-9 antibody|MGC99577 antibody|MRXE antibody|MSTP009 antibody|N14F antibody|Renin receptor antibody|Renin/prorenin receptor antibody|RENR_HUMAN antibody|V ATPase M8 9 subunit antibody|V ATPase M8.9 subunit antibody|V-ATPase M8.9 subunit antibody|Vacuolar ATP synthase membrane sector associated protein M8 9 antibody|Vacuolar ATP synthase membrane sector-associated protein M8-9 antibody|vacuolar proton ATP synthase membrane sector associated protein M8 9 antibody|XMRE antibody
Anti-ATP6IP2 antibody (ab40790)
Close sc-67390|sc-55025|

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-5000,IHC:1:20-1:200

Recommended protocols: check protocols


Anti-ATP6AP2 Antibody

Catalogue No.



Human, Mouse


Recombinant human Renin receptor protein (251-350AA)





Recommended dilution

Recommended dilution:WB:1:500-5000,IHC:1:20-1:200







Molecular weight

39 kDa


Antigen Affinity Purified


Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:418573( Chicken), Entrez Gene:513520( Cow), Entrez Gene:10159( Human), Entrez Gene:70495( Mouse), Entrez Gene:302526( Rat), Omim:300556( Human), SwissProt:P81134( Cow), SwissProt:O75787( Human), SwissProt:Q9CYN9( Mouse), SwissProt:Q6AXS4( Rat), Unigene:495960( Human), Unigene:25148( Mouse), Unigene:12944( Rat)

Protein function

Functions as a renin and prorenin cellular receptor. May mediate renin-dependent cellular responses by activating ERK1 and ERK2. By increasing the catalytic efficiency of renin in AGT/angiotensinogen conversion to angiotensin I, it may also play a role in the renin-angiotensin system (RAS). .

Protein tissue specificity

Expressed in brain, heart, placenta, liver, kidney and pancreas. Barely detectable in lung and skeletal muscles. In the kidney cortex it is restricted to the mesangium of glomeruli. In the coronary and kidney artery it is expressed in the subendothelium, associated to smooth muscles where it colocalizes with REN. Expressed in vascular structures and by syncytiotrophoblast cells in the mature fetal placenta. .

Involvement in disease

Mental retardation, X-linked, with epilepsy (MRXE) [MIM:300423]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRXE patients manifest mild to moderate mental retardation associated with epilepsy, delays in motor milestones and speech acquisition in infancy. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Parkinsonism with spasticity, X-linked (XPDS) [MIM:300911]: A syndrome characterized by parkinsonian features, such as cogwheel rigidity, resting tremor and bradykinesia, and variably penetrant spasticity. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein post-translational modifications

Phosphorylated. .

Protein cellular localization

Membrane ; Single-pass type I membrane protein .

Research area

All research areas>Membrane Receptors>Renin Receptor
(View all antibody categories related to Membrane Receptors)


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Product type

Primary antibody


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