C10orf2 Antikörper (C-Term)
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- Target Alle C10orf2 (C10ORF2) Antikörper anzeigen
- C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
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Bindungsspezifität
- AA 656-684, C-Term
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C10orf2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Aufreinigung
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogen
- This C10orf2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 656-684 amino acids from the C-terminal region of human C10orf2.
- Klon
- RB32016
- Isotyp
- Ig Fraction
- Top Product
- Discover our top product C10ORF2 Primärantikörper
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- Applikationshinweise
- WB: 1:1000. IHC-P: 1:10~50
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- C10orf2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
- Haltbarkeit
- 6 months
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- Target
- C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
- Andere Bezeichnung
- C10orf2 (C10ORF2 Produkte)
- Synonyme
- ATXN8 antikoerper, IOSCA antikoerper, MTDPS7 antikoerper, PEO antikoerper, PEO1 antikoerper, PEOA3 antikoerper, SANDO antikoerper, SCA8 antikoerper, TWINL antikoerper, C6H10orf2 antikoerper, D19Ertd626e antikoerper, Twinl antikoerper, twinkle mtDNA helicase L homeolog antikoerper, twinkle mtDNA helicase antikoerper, twnk.L antikoerper, TWNK antikoerper, Twnk antikoerper
- Hintergrund
- This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
- Molekulargewicht
- 77154
- Gen-ID
- 56652
- NCBI Accession
- NP_001157284, NP_068602
- UniProt
- Q96RR1
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