IFT43 anticorps (AA 111-208) (FITC)
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- Antigène Voir toutes IFT43 Anticorps
- IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
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Épitope
- AA 111-208
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp IFT43 est conjugé à/à la FITC
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 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
- Top Product
- Discover our top product IFT43 Anticorps primaire
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- 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
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- 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
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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
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