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Recombinant Human ATP5F1A

CAT: 0710-P9285-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0710-P9285-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Product Name Alternative
ATP synthase subunit alpha, mitochondrial, ATP synthase F1 subunit alpha, ATP5A, ATP5A1
UniProt
P25705
Expression Region
44-553
Host
E.Coli
Tag
N-terminal His-IF2DI Tag
Applications
Western Blot, ELISA
Field of Research
Metabolism
Purity
Greater than 90% as determined by SDS-PAGE.
Form
Lyophilized powder
Reconstitution
Centrifuge the vial before opening, reconstitute in sterile distilled water to a concentration of 0.1-1 mg/ml by gently pipetting 2-3 times, don't vortex.
Molecular Weight
75.8 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
The lyophilized protein is stable at -20 °C for up to 1 year. For extended storage, it is recommended to further dilute in working aliquots after reconstitution. The protein solution is stable at ≤ -20 °C for 3 months, or 2-7 days at 2-8 °C under sterile conditions.Avoid repeated freeze/thaw cycle.
Formulation
Lyophilized from a 0.2 μm filtered solution of 10 mM Hepes, 150 mM NaCl with 5% trehalose, pH 7.4.
Organism Species
Human

UniProtKB · P25705

ATP synthase F(1) complex subunit alpha, mitochondrial

ATPA_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P25705
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ATP5F1A
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
A8K092, B4DY56, K7ENP3, Q53XX6, Q8IXV2, Q96FB4, Q96HW2, Q96IR6, Q9BTV8
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationGlycoproteinMethylationPhosphoprotein

Coding sequence diversity

Alternative splicing

Biological process

ATP synthesisHydrogen ion transportIon transportTransport

Ligand

ATP-bindingNucleotide-binding

Cellular component

Cell membraneCF(1)MembraneMitochondrionMitochondrion inner membrane

Disease

Disease variantPrimary mitochondrial disease

Domain

Transit peptide

Molecular function

Translocase

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