Catalog No.
YHK96601
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Ile103-Thr208
Predicted molecular weight
24.57 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q96FT9
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
C14orf179, IFT43, Intraflagellar transport protein 43 homolog
Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol., PMID:39090729
Identification of the principal neuropeptide MIP and its action pathway in larval settlement of the echiuran worm Urechis unicinctus., PMID:38641568
Reanalysis of Whole-Exome Sequencing Data of an Infant with Suspected Diagnosis of Jeune Syndrome Revealed a Likely Pathogenic Variant in GRK2: A Newly Associated Gene for Jeune Syndrome Phenotype., PMID:38585547
Clinical report and genetic analysis of rare premature infant nephronophthisis caused by biallelic TTC21B variants., PMID:38439578
A whole exome sequencing study to identify rare variants in multiplex families with alcohol use disorder., PMID:37915799
Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia., PMID:33517396
Primary ciliary dyskinesia relative protein ZMYND10 is involved in regulating ciliary function and intraflagellar transport in Paramecium tetraurelia., PMID:33279757
The microgravity induces the ciliary shortening and an increased ratio of anterograde/retrograde intraflagellar transport of osteocytes., PMID:32828281
Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35., PMID:32804427
Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease., PMID:32007091
A new case of KIAA0753-related variant of Jeune asphyxiating thoracic dystrophy., PMID:31816441
Ttc39c is upregulated during skeletal muscle atrophy and modulates ERK1/2 MAP kinase and hedgehog signaling., PMID:31188487
[Clinical features and mutational analysis of a case with Sensenbrenner syndrome]., PMID:29896747
Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis., PMID:29220510
Clinical and molecular genetic characterization of a male patient with Sensenbrenner syndrome (cranioectodermal dysplasia) and biallelic WDR35 mutations., PMID:29134781
A mutation in IFT43 causes non-syndromic recessive retinal degeneration., PMID:28973684
Dynein-Driven Retrograde Intraflagellar Transport Is Triphasic in C. elegans Sensory Cilia., PMID:28479320
IFT54 regulates IFT20 stability but is not essential for tubulin transport during ciliogenesis., PMID:28417161
Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia., PMID:28400947
Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations., PMID:28332779
Functional exploration of the IFT-A complex in intraflagellar transport and ciliogenesis., PMID:28207750
Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors., PMID:27932497
De novo 14q24.2q24.3 microdeletion including IFT43 is associated with intellectual disability, skeletal anomalies, cardiac anomalies, and myopia., PMID:26892345
Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum., PMID:26792575
Regulation of cilium length and intraflagellar transport by the RCK-kinases ICK and MOK in renal epithelial cells., PMID:25243405
The Small GTPase Rsg1 is important for the cytoplasmic localization and axonemal dynamics of intraflagellar transport proteins., PMID:24192041
Ciliary disorder of the skeleton., PMID:22791528
Subunit interactions and organization of the Chlamydomonas reinhardtii intraflagellar transport complex A proteins., PMID:22170070
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome., PMID:21378380
For research use only. Not for human or drug use.
