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NDUFS2 Antibody

CAT: 0864-A29555-100UGSize: 100 µgDry Ice: NoHazardous: No
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CAT#:0864-A29555-100UGSize:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
CI 49, CI 49kD, CI-49kD, Complex 1, mitochondrial respiratory chain, 49 KD subunit, Complex I 49kD, Complex I 49kDa subunit, Complex I-49kD, mitochondrial, NADH dehydrogenase (ubiquinone) Fe S protein 2 49kDa, NADH dehydrogenase (ubiquinone) Fe S protein 2, 49kDa (NADH coenzyme Q reductase) , NADH dehydrogenase [ubiquinone] iron sulfur protein 2, mitochondrial, NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, NADH ubiquinone oxidoreductase 49 kDa subunit, NADH ubiquinone oxidoreductase NDUFS2 subunit, NADH-ubiquinone oxidoreductase 49 kDa subunit, NADH:ubiquinone oxidoreductase core subunit S2, Ndufs2, NDUS2_HUMAN
UniProt
O75306
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Rat, Mouse
Target Antigen
Recombinant Human NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial protein (297-427AA)
Target
NDUFS2
Clonality
Polyclonal
Conjugation
Non-conjugated
Applications
ELISA, WB, IHC
Field of Research
Tags & Cell Markers
Purification Method
>95%, Protein G purified
Form
Liquid
Buffer
0.03% Proclin 300, 50% glycerol, 0.01M PBS, pH 7.4.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · O75306

NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial

NDUS2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O75306
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
NDUFS2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
7.1.1.2
Processing
Precursor
Secondary accessions
D3DVG7, J3KPM7, Q5VTW0, Q969P3, Q9UEV3
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Ligand

4Fe-4SIronIron-sulfurMetal-bindingNADUbiquinone

PTM

AcetylationMethylation

Coding sequence diversity

Alternative splicing

Disease

Disease variantLeber hereditary optic neuropathyPrimary mitochondrial disease

Biological process

Electron transportRespiratory chainTransport

Cellular component

MembraneMitochondrionMitochondrion inner membrane

Molecular function

OxidoreductaseTranslocase

Domain

Transit peptide

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