Products for Research Use Only

NFU1 Rabbit Polyclonal Antibody

CAT: 0013-GTR18677747Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18677747Size:100 µg
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Description
NFU1 Rabbit Polyclonal Antibody
Product Name Alternative
NFU1; HIRIP5; CGI-33; NFU1 iron-sulfur cluster scaffold homolog, mitochondrial; HIRA-interacting protein 5
UniProt
Q9UMS0
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
E.coli-derived human NFU1 recombinant protein (Position: Q42-P254) . Human NFU1 shares 93% amino acid (aa) sequence identity with mouse NFU1.
Target
NFU1 iron-sulfur cluster scaffold homolog, mitochondrial
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
Immunogen affinity purified.
Concentration
Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Dilution
Western blot, 0.25-0.5 μg/ml, Human, Mouse, Rat Immunocytochemistry/Immunofluorescence, 5 μg/ml, Human Flow Cytometry (Fixed), 1-3 μg/1x10^6 cells, Human ELISA, 0.1-0.5 μg/ml
Form
Lyophilized
Molecular Weight
28 kDa
Storage Conditions
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
Notes
For research use only.
Tested Applications
ELISA, FC, ICC, WB
Host or Source
Rabbit
Preservative
Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Isotype
Rabbit IgG

UniProtKB · Q9UMS0

NFU1 iron-sulfur cluster scaffold homolog, mitochondrial

NFU1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9UMS0
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
NFU1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
B4DUL9, Q53QE5, Q6VNZ8, Q7Z5B1, Q7Z5B2, Q9Y322
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

CytoplasmMitochondrion

Disease

Disease variantHereditary spastic paraplegiaNeurodegenerationPrimary mitochondrial disease

Ligand

IronIron-sulfurMetal-binding

Domain

Transit peptide