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Mouse Anti-ATP5F1A Recombinant Antibody (7F9BG1) (CBMAB-1168-CN)

This product is a mouse antibody that recognizes ATP5F1A of human. The antibody 7F9BG1 can be used for immunoassay techniques such as: WB, FC, ICC, IF.
See all ATP5F1A antibodies
Published Data
Fig.1 LDGs from individuals with CGD release NETs in a mitochondrial superoxide-dependent manner.
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Fig.2 Cell surface staining of TOM20 in non-fixed neutrophils upon activation with the stimuli shown.
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Fig.3 The same mitochondria preparations used in were analyzed. Proteins were stained with anti-a, anti-b, and anti-MLQ antibodies.
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Summary

Host Animal
Mouse
Specificity
Human, Cattle, Mouse, Rat
Clone
7F9BG1
Antibody Isotype
IgG2b, κ
Application
WB, ICC, IF, FC

Basic Information

Immunogen
Bovine Complex V.
Host Species
Mouse
Specificity
Human, Cattle, Mouse, Rat
Antibody Isotype
IgG2b, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
WB1 µg/ml
IF(ICC)1-5 µg/ml
FC1 µg/ml

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
HEPES
Preservative
0.02% sodium azide
Concentration
1 mg/ml
Storage
Store at +4°C. Do not freeze.

Target

Full Name
ATP Synthase F1 Subunit Alpha
Introduction
This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, using an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. Mitochondrial membrane ATP synthase (F1F0 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.
Entrez Gene ID
Human498
Mouse11946
Rat65262
Cattle282578
UniProt ID
HumanP25705
MouseQ03265
RatP15999
CattleP19483
Alternative Names
OMR; ORM; ATPM; MOM2; ATP5A; hATP1; ATP5A1; MC5DN4; ATP5AL2; COXPD22; HEL-S-123m
Function
Mitochondrial membrane ATP synthase (F1F0 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, F1 - containing the extramembraneous catalytic core, and F0 - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F1 is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Subunits alpha and beta form the catalytic core in F1. Rotation of the central stalk against the surrounding alpha3beta3 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-binding sites (By similarity).
Binds the bacterial siderophore enterobactin and can promote mitochondrial accumulation of enterobactin-derived iron ions (PubMed:30146159).
Biological Process
ATP biosynthetic process Source: CAFA
ATP synthesis coupled proton transport Source: GO_Central
Cristae formation Source: Reactome
Lipid metabolic process Source: UniProtKB
Mitochondrial ATP synthesis coupled proton transport Source: UniProtKB
Negative regulation of endothelial cell proliferation Source: UniProtKB
Positive regulation of blood vessel endothelial cell migration Source: CAFA
Cellular Location
Mitochondrion; Mitochondrion inner membrane; Cell membrane. Colocalizes with HRG on the cell surface of T-cells (PubMed:19285951).
Involvement in disease
Combined oxidative phosphorylation deficiency 22 (COXPD22): A mitochondrial disorder characterized by intrauterine growth retardation, microcephaly, hypotonia, pulmonary hypertension, failure to thrive, encephalopathy, and heart failure.
Mitochondrial complex V deficiency, nuclear type 4 (MC5DN4): 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.
PTM
The N-terminus is blocked.
Acetylated on lysine residues. BLOC1S1 is required for acetylation.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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