Catalog No.
YHK95601
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Met1-Asp133
Predicted molecular weight
17.82 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q96LK0
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
Centrosomal protein of 19 kDa, C3orf34, Cep19, CEP19
Architecture of RabL2-associated complexes at the ciliary base: A structural modeling perspective: Deciphering the structural organization of ciliary RabL2 complexes., PMID:38991980
Severe Early-Onset Obesity and Diabetic Ketoacidosis due to a Novel Homozygous c.169C>T p.Arg57* Variant in CEP19 Gene., PMID:38585545
The IFT81-IFT74 complex acts as an unconventional RabL2 GTPase-activating protein during intraflagellar transport., PMID:37606072
CEP19-RABL2-IFT-B axis controls BBSome-mediated ciliary GPCR export., PMID:36074075
Comparative transcriptome provides insights into the selection adaptation between wild and farmed foxes., PMID:34646484
Analysis of the "centrosome-ome" identifies MCPH1 deletion as a cause of centrosome amplification in human cancer., PMID:32681070
RABL2 positively controls localization of GPCRs in mammalian primary cilia., PMID:30578315
A distal centriolar protein network controls organelle maturation and asymmetry., PMID:30258116
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly., PMID:29127258
Gating Ciliary Transport., PMID:28697332
CEP19 cooperates with FOP and CEP350 to drive early steps in the ciliogenesis programme., PMID:28659385
The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base., PMID:28625565
RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly., PMID:28428259
Morbid obesity resulting from inactivation of the ciliary protein CEP19 in humans and mice., PMID:24268657
For research use only. Not for human or drug use.
