IFT43 anticorps (AA 111-208) (FITC)

N° du produit ABIN1710539

Détail du produit anti-IFT43 anticorps (FITC)

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

Épitope: AA 111-208

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IFT43 est conjugé à/à la FITC

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

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human IFT43

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur IFT43

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

Autre désignation: Ift43 (IFT43 Produits)

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

Sujet:

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: Signalisation Hedgehog