IFT43 antibody (AA 111-208) (FITC)
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- Target See all IFT43 Antibodies
- IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
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Binding Specificity
- AA 111-208
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This IFT43 antibody is conjugated to FITC
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Predicted Reactivity
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human IFT43
- Isotype
- IgG
- Top Product
- Discover our top product IFT43 Primary Antibody
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- Application Notes
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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.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
- Alternative Name
- Ift43 (IFT43 Products)
- Synonyms
- C10H14orf179 antibody, C14orf179 antibody, CED3 antibody, 1700019E19Rik antibody, R75064 antibody, c14orf179 antibody, RGD1307392 antibody, intraflagellar transport 43 antibody, intraflagellar transport 43 L homeolog antibody, intraflagellar transport 43 homolog (Chlamydomonas) antibody, IFT43 antibody, Ift43 antibody, ift43.L antibody
- Background
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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
- Hedgehog Signaling
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