IFT43 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2714061

Détail du produit

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

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette IFT43 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human Chromosome 14 open reading frame 179 (C14orf179), transcript variant 1 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

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

Autre désignation: Chromosome 14 Open Reading Frame 179 (c14orf179) (IFT43 Produits)

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

Sujet: This 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.

Poids moléculaire: 23.7 kDa

NCBI Accession: NP_443105

Pathways: Signalisation Hedgehog