FIGNL1 Antikörper (AbBy Fluor® 555)
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- Target Alle FIGNL1 Antikörper anzeigen
- FIGNL1 (Fidgetin-Like 1 (FIGNL1))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FIGNL1 Antikörper ist konjugiert mit AbBy Fluor® 555
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FIGNL1
- Isotyp
- IgG
- Top Product
- Discover our top product FIGNL1 Primärantikörper
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- Applikationshinweise
- IF(IHC-P) 1:50-200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- FIGNL1 (Fidgetin-Like 1 (FIGNL1))
- Andere Bezeichnung
- FIGNL1 (FIGNL1 Produkte)
- Synonyme
- fb82h05 antikoerper, wu:fb82h05 antikoerper, wu:fj99a11 antikoerper, zgc:193664 antikoerper, fidgetin like 1 antikoerper, fidgetin-like 1 antikoerper, fidgetin-like 1 L homeolog antikoerper, FIGNL1 antikoerper, fignl1 antikoerper, Fignl1 antikoerper, fignl1.L antikoerper
- Hintergrund
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Synonyms: Fidgetin like protein 1, fidgetin-like 1, FIGL1_HUMAN.
Background: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
- Gen-ID
- 63979
- Pathways
- Microtubule Dynamics
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