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Rabbit Anti-ATP6AP2 Antibody (CSB-PA002384ESR2HU)
Supplier: CUSABIO BIOTECH CO.
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 AntibodyMore 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)
Anti-ATP6IP2 antibody (ab40790)
Recommended applications: ELISA, WB, IHC
Recommended dilution: Recommended dilution:WB:1:500-5000,IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Renin receptor protein (251-350AA)
ELISA, WB, IHC
|Recommended dilution|| |
|Molecular weight|| |
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|| |
|Protein cellular localization|| |
Membrane ; Single-pass type I membrane protein .
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|Product type|| |
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