IFT43 antibody (AA 111-208) (Cy7)

Catalog No. ABIN1708728

Product Details anti-IFT43 Antibody (Cy7)

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

Binding Specificity: AA 111-208

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IFT43 antibody is conjugated to Cy7

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

Application Details

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

Restrictions: For Research Use only

Handling

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

Target Details for IFT43

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:

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