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OXA1L antibody

CAT: 0710-FNab06048Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0710-FNab06048Size:100 µg
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Background
This gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N-terminal tail of subunit 2 of cytochrome c oxidase, and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain.
Synonyms
Mitochondrial inner membrane protein OXA1L|Hsa|OXA1Hs|Oxidase assembly 1-like protein (OXA1-like protein) |OXA1L
Gene ID
5018
UniProt
Q15070
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Oxidase (cytochrome c) assembly 1-like
Target
OXA1L
Clonality
Polyclonal
Isotype
IgG
Applications
ELISA, WB, IHC
Field of Research
Signal Transduction, Metabolism
Purification
Immunogen affinity purified
Dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:100
Purity
≥95% as determined by SDS-PAGE
Form
Liquid
Molecular Weight
42 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Tested Applications
ELISA, WB, IHC

UniProtKB · Q15070

Mitochondrial inner membrane protein OXA1L

OXA1L_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q15070
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
OXA1L
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
A0A087X0L7, B4DPA2
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

MembraneMitochondrionMitochondrion inner membrane

PTM

Phosphoprotein

Domain

Transit peptideTransmembraneTransmembrane helix