IFT43 Antikörper (AA 111-208) (Cy5.5)

Produktnummer ABIN1706917

Produktdetails anti-IFT43 Antikörper (Cy5.5)

Target: IFT43 (Intraflagellar Transport 43 Homolog (IFT43))

Bindungsspezifität: AA 111-208

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser IFT43 Antikörper ist konjugiert mit Cy5.5

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human IFT43

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Details zu IFT43

Target: IFT43 (Intraflagellar Transport 43 Homolog (IFT43))

Andere Bezeichnung: Ift43 (IFT43 Produkte)

Synonyme: C10H14orf179 antikoerper, C14orf179 antikoerper, CED3 antikoerper, 1700019E19Rik antikoerper, R75064 antikoerper, c14orf179 antikoerper, RGD1307392 antikoerper, intraflagellar transport 43 antikoerper, intraflagellar transport 43 L homeolog antikoerper, intraflagellar transport 43 homolog (Chlamydomonas) antikoerper, IFT43 antikoerper, Ift43 antikoerper, ift43.L antikoerper

Hintergrund:

Synonyms: C14orf179, t43, T43_HUMAN, Intraflagellar transport protein 43 homolog.

Background: IFT43 is a gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Pathways: Hedgehog Signalweg