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Antibodies
Anti-ATP5A Antibody
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产品名称:
Anti-ATP5A Antibody
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简单介绍
Anti-ATP5A
Antibody
Anti-ATP5A Antibody
的详细介绍
Overview
Name:
Anti-ATP5A
Antibody
See all ATP5A primary antibodies
Description:
Rabbit polyclonal antibody to ATP5A
Specificity:
ATP5A Polyclonal Antibody detects endogenous levels of ATP5A protein.
Applications:
WB, IHC, ELISA
Reactivity:
Human, Mouse, Rat
Immunogen:
Synthesized peptide derived from the Internal region of human ATP5A.
Host:
Rabbit
Clonality:
Polyclonal
Conjugate:
Unconjugated
Purification:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration:
1mg / ml
Formulation:
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage:
Store at -20?C / 1 year
Target
Function:
Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Subunits alpha and beta form the catalytic core in F(1). Rotation of the central stalk against the surrounding alpha(3)beta(3) subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits. Subunit alpha does not bear the catalytic high-affinity ATP-s (By similarity).
Tissue Specificity:
Fetal lung, heart, liver, gut and kidney. Expressed at higher levels in the fetal brain, retina and spinal cord.
Involvement in Disease:
Combined oxidative phosphorylation deficiency 22: A mitochondrial disorder characterized by intrauterine growth retardation, microcephaly, hypotonia, pulmonary hypertension, failure to thrive, encephalopathy, and heart failure.
Mitochondrial complex V deficiency, nuclear 4: A mitochondrial disorder with heterogeneous clinical manifestations including dysmorphic features, psychomotor retardation, hypotonia, growth retardation, cardiomyopathy, enlarged liver, hypoplastic kidneys and elevated lactate levels in urine, plasma and cerebrospinal fluid.
Sequence Similarities:
Belongs to the ATPase alpha/beta chains family.
Post-Translational Modification:
The N-terminus is blocked.
Cellular Location:
Mitochondrion inner membrane. Cell membrane.
Colocalizes with HRG on the cell surface of T-cells (PubMed:19285951).
Database Links:
Entrez Gene: 498?Human
Entrez Gene: 11946?Mouse
Entrez Gene: 65262?Rat
Omim: 164360?Human
SwissProt: P25705?Human
SwissProt: Q03265?Mouse
SwissProt: P15999?Rat
Unigene: 298280?Human
Unigene: 276137?Mouse
Unigene: 474505?Mouse
Unigene: 40255?Rat
Synonyms:
ATP synthase alpha chain, mitochondrial Antibody
ATP synthase subunit alpha Antibody
ATP synthase subunit alpha mitochondrial Antibody
ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle Antibody
ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, 1 Antibody
ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform 1, cardiac muscle Antibody
ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform 2, non-cardiac muscle-like 2 Antibody
ATP sythase (F1 ATPase) alpha subunit Antibody
ATP5A Antibody
Atp5a1 Antibody
ATP5AL2 Antibody
ATPA_HUMAN Antibody
ATPM Antibody
Epididymis secretory sperm binding protein Li 123m Antibody
hATP1 Antibody
HEL-S-123m Antibody
MC5DN4 Antibody
mitochondrial Antibody
Mitochondrial ATP synthetase Antibody
Mitochondrial ATP synthetase oligomycin resistant Antibody
Modifier of Min 2 mouse homolog Antibody
Modifier of Min 2, mouse, homolog of Antibody
MOM2 Antibody
OMR Antibody
ORM Antibody
OTTHUMP00000163475 Antibody
Information:
Target information shown above is from the UniProt Consortium.
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