RBFA Antikörper
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- Target Alle RBFA Antikörper anzeigen
- RBFA (Ribosome Binding Factor A (RBFA))
- Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser RBFA Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human RBFA
- Isotyp
- IgG
- Top Product
- Discover our top product RBFA Primärantikörper
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- RBFA (Ribosome Binding Factor A (RBFA))
- Andere Bezeichnung
- RBFA (RBFA Produkte)
- Synonyme
- C18orf22 antikoerper, HsT169 antikoerper, 1110032A13Rik antikoerper, AI595940 antikoerper, RGD1311910 antikoerper, zgc:162590 antikoerper, ribosome binding factor A antikoerper, RBFA antikoerper, Rbfa antikoerper, rbfa antikoerper
- Hintergrund
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Synonyms: mitochondrial, C18orf25, Chromosome 18 open reading frame 22, HsT169, Hypothetical protein LOC79863, Putative ribosome binding factor A, mitochondrial precursor, Putative ribosome-binding factor A, rbfA, RBFA_HUMAN.
Background: C18orf22, also known as HsT169, is a 343 amino acid protein that localizes to the mitochondrion and is expressed as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
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