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IBA57 Antibody

CAT: 0399-CSB-PA722566LA01HU-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0399-CSB-PA722566LA01HU-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Gene Aliases
C1orf69 antibody; CAF17_HUMAN antibody; Chromosome 1 open reading frame 69 antibody; FLJ12734 antibody; FLJ13849 antibody; IBA57 antibody; IBA57 homolog iron sulfur cluster assembly antibody; IBA57 iron sulfur cluster assembly homolog antibody; IBA57 iron sulfur cluster assembly homolog (S. cerevisiae) antibody; IBA57; S. cerevisiae; homolog of antibody; Iron sulfur cluster assembly factor for biotin synthase and aconitase like antibody; iron-sulfur cluster assembly factor for biotin synthase- and aconitase-like mitochondrial proteins; with a mass of 57kDa antibody; Iron-sulfur cluster assembly factor homolog antibody; Mitochondrial proteins with a mass of 57kDa antibody; MMDS3 antibody; Putative transferase C1orf69 mitochondrial antibody; Putative transferase CAF17; mitochondrial antibody; SPG74 antibody
UniProt
Q5T440
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Mouse
Target Antigen
Recombinant Human Putative transferase CAF17, mitochondrial protein (286-356AA)
Target
IBA57
Clonality
Polyclonal
Conjugation
Non-conjugated
Field of Research
Others
Purification Method
>95%, Protein G purified
Form
Liquid
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Antibody Type
Polyclonal Antibody
Tested Applications
ELISA, WB, IHC, IF; Recommended dilution: WB:1:500-1:5000, IHC:1:200-1:500, IF:1:50-1:200
Isotype
IgG

UniProtKB · Q5T440

Iron-sulfur cluster assembly factor IBA57, mitochondrial

CAF17_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q5T440
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
IBA57
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
—
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

Acetylation

Disease

Disease variantHereditary spastic paraplegiaNeurodegenerationPrimary mitochondrial disease

Biological process

Heme biosynthesis

Cellular component

Mitochondrion

Domain

Transit peptide

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