| Description : |
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants. |
| Source : |
HEK293 |
| Species : |
Human |
| Tag : |
Myc/DDK |
| Molecular Mass : |
58.3 kDa |
| AA Sequence : |
MAEERVATRTQFPVSTESQKPRQKK APEFPILEKQNWLIHLHYIRKDYEA CKAVIKEQLQETQGLCEYAIYVQAL IFRLEGNIQESLELFQTCAVLSPQS ADNLKQVARSLFLLGKHKAAIEVYN EAAKLNQKDWEISHNLGVCYIYLKQ FNKAQDQLHNALNLNRHDLTYIMLG KIHLLEGDLDKAIEVYKKAVEFSPE NTELLTTLGLLYLQLGIYQKAFEHL GNALTYDPTNYKAILAAGSMMQTHG DFDVALTKYRVVACAVPESPPLWNN IGMCFFGKKKYVAAISCLKRANYLA PFDWKILYNLGLVHLTMQQYASAFH FLSAAINFQPKMGELYMLLAVALTN LEDTENAKRAYAEAVHLDKCNPLVN LNYAVLLYNQGEKKNALVQYQEMEK KVSLLKDNSSLEFDSEMVEMAQKLG AALQVGEALVWTKPVKDPKSKHQTT STSKPASFQQPLGSNQALGQAMSSA AAYRTLPSGAGGTSQFTKPPSLPLE PEPAVESSPTETSEQIREKTRTRPL EQKLISEEDLAANDILDYKDDDDKV |
| Purity : |
> 80% as determined by SDS-PAGE and Coomassie blue staining |
| Stability : |
Stable for 3 months from receipt of products under proper storage and handling conditions. |
| Storage : |
Store at -80 centigrade. Avoid repeated freeze-thaw cycles. |
| Concentration : |
50 μg/mL as determined by BCA |
| Storage Buffer : |
100 mM glycine, 25 mM Tris-HCl, pH 7.3. |
