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Antibodies
Anti-ATP5A1 Antibody
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产品名称:
Anti-ATP5A1 Antibody
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简单介绍
Anti-ATP5A1
Antibody
Anti-ATP5A1 Antibody
的详细介绍
Overview
Name:
Anti-ATP5A1
Antibody
See all ATP5A1 primary antibodies
Description:
Rabbit polyclonal antibody to ATP5A1
Specificity:
The antibody detects endogenous level of total ATP5A1 antibody.
Applications:
WB, IF
Reactivity:
Human, Mouse, Rat
Immunogen:
Recombinant protein of human ATP5A1.
Host:
Rabbit
Clonality:
Polyclonal
Conjugate:
Unconjugated
Purification:
Antibodies were purified by affinity purification using immunogen.
Concentration:
1.0mg / ml
Formulation:
Supplied at 1.0mg / mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Storage:
Store at -20˚C
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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