IBA57 antibody (Middle Region)
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- Target See all IBA57 Antibodies
- IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
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Binding Specificity
- Middle Region
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This IBA57 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- SPEACGAASL QERAGAAAIL IRDPRTARMG WRLLTQDEGP ALVPGGRLGD
- Purification
- Affinity purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human IBA57
- Top Product
- Discover our top product IBA57 Primary Antibody
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anti-IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57) (AA 286-356) antibody
IBA57 Reactivity: Human WB, ELISA, IHC, IF Host: Rabbit Polyclonal unconjugated
anti-IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57) (AA 131-230) antibodyIBA57 Reactivity: Rat WB, IF (cc), IF (p), ELISA, IHC (p), IHC (fro), ICC Host: Rabbit Polyclonal unconjugated
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 23 % sucrose.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- 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.
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- Target
- IBA57 (IBA57, Iron-Sulfur Cluster Assembly Homolog (IBA57))
- Alternative Name
- IBA57 (IBA57 Products)
- Synonyms
- C1orf69 antibody, 4930543L23Rik antibody, A230051G13Rik antibody, zgc:153540 antibody, IBA57 homolog, iron-sulfur cluster assembly antibody, IBA57 antibody, Iba57 antibody, iba57 antibody
- Background
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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 - Gene ID
- 200205
- NCBI Accession
- NM_001010867, NP_001010867
- UniProt
- Q5T440
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