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IBA57 anticorps (Middle Region)
IBA57
Reactivité: Humain
WB
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN5518034
Détail du produit anti-IBA57 anticorps
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Antigène
Voir toutes IBA57 Anticorps
IBA57
(IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
Épitope
Tous les épitopes à travers IBA57 Anticorps.
Middle Region
Reactivité
Toutes les réactivités sur IBA57 Anticorps
Humain
Hôte
Toutes les hôtes sur IBA57 Anticorps
Lapin
Clonalité
Toutes les clonalités sur IBA57 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers IBA57 Anticorps
Cet anticorp IBA57 est non-conjugé
Application
Tous les applications à travers IBA57 Anticorps.
Western Blotting (WB)
Séquence
QDEGPALVPG GRLGDLWDYH QHRYLQGVPE GVRDLPPGVA LPLESNLAFM
Purification
Affinity purified
Immunogène
The immunogen is a synthetic peptide directed towards the middle region of human C1ORF69
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Information d'application
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Indications d'application
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Stockage
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Format
Liquid
Buffer
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
Agent conservateur
Sodium azide
Précaution d'utilisation
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Stock
-20 °C
Stockage commentaire
For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
Détails sur IBA57
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Antigène
IBA57
(IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
Autre désignation
C1ORF69 (IBA57 Produits )
Synonymes
anticorps C1orf69, anticorps 4930543L23Rik, anticorps A230051G13Rik, anticorps zgc:153540, anticorps IBA57 homolog, iron-sulfur cluster assembly, anticorps IBA57, anticorps Iba57, anticorps iba57
Sujet
The protein encoded by this gene localizes to the mitochondrion and is part of the iron-sulfur cluster assembly pathway. The encoded protein functions late in the biosynthesis of mitochondrial 4Fe-4S proteins. Defects in this gene have been associated with autosomal recessive spastic paraplegia-74 and with multiple mitochondrial dysfunctions syndrome-3. Two transcript variants encoding different isoforms have been found for this gene. The smaller isoform is not likely to be localized to the mitochondrion since it lacks the amino-terminal transit peptide. Alias Symbols: MMDS3, SPG74, C1orf69 Protein Size: 356
ID gène
200205
NCBI Accession
NM_001010867 , NP_001010867
UniProt
Q5T440
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