IFT43 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
-
- Target See all IFT43 Proteins
- IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 1
-
Origin
- Human
-
Source
- HEK-293 Cells
- Purification tag / Conjugate
- This IFT43 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
-
- 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
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product IFT43 Protein
-
-
- Application Notes
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
-
The tag is located at the C-terminal.
- Restrictions
- For Research Use only
-
- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- 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.
-
- Target
- IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
- Alternative Name
- Chromosome 14 Open Reading Frame 179 (c14orf179) (IFT43 Products)
- Synonyms
- 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
- Background
- 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.
- Molecular Weight
- 23.7 kDa
- NCBI Accession
- NP_443105
- Pathways
- Hedgehog Signaling
-