IFT43 antibody (AA 111-208) (HRP)

Catalog No. ABIN1712353

This Rabbit Polyclonal antibody specifically detects IFT43 in WB, IHC (p) and IHC (fro). It exhibits reactivity toward Human.

Quick Overview for IFT43 antibody (AA 111-208) (HRP) (ABIN1712353)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IFT43 antibody is conjugated to HRP

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-IFT43 Antibody (HRP)

Binding Specificity: AA 111-208

Purpose: IFT43 Polyclonal Antibody, HRP Conjugated

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: WB(1:300-5000),

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, 0.02 % 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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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: T43

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