| Description : |
COPG2 (COPI Coat Complex Subunit Gamma 2) is a Protein Coding gene. Diseases associated with COPG2 include Silver-Russell Syndrome 1 and Autism. Among its related pathways are Transport to the Golgi and subsequent modification and Metabolism of proteins. Gene Ontology (GO) annotations related to this gene include binding and structural molecule activity. An important paralog of this gene is COPG1. |
| Source : |
HEK293 |
| Species : |
Human |
| Tag : |
Myc/DDK |
| Molecular Mass : |
97.4 kDa |
| AA Sequence : |
MIKKFDKKDEESGSGSNPFQHLEKS AVLQEARIFNETPINPRRCLHILTK ILYLLNQGEHFGTTEATEAFFAMTR LFQSNDQTLRRMCYLTIKEMATISE DVIIVTSSLTKDMTGKEDVYRGPAI RALCRITDGTMLQAIERYMKQAIVD KVSSVSSSALVSSLHMMKISYDVVK RWINEAQEAASSDNIMVQYHALGVL YHLRKNDRLAVSKMLNKFTKSGLKS QFAYCMLIRIASRLLKETEDGHESP LFDFIESCLRNKHEMVIYEAASAII HLPNCTARELAPAVSVLQLFCSSPK PALRYAAVRTLNKVAMKHPSAVTAC NLDLENLITDSNRSIATLAITTLLK TGSESSVDRLMKQISSFVSEISDEF KVVVVQAISALCQKYPRKHSVMMTF LSNMLRDDGGFEYKRAIVDCIISIV EENPESKEAGLAHLCEFIEDCEHTV LATKILHLLGKEGPRTPVPSKYIRF IFNRVVLENEAVRAAAVSALAKFGA QNESLLPSILVLLQRCMMDTDDEVR DRATFYLNVLQQRQMALNATYIFNG LTVSVPGMEKALHQYTLEPSEKPFD MKSIPLAMAPVFEQKAEITLVATKP EKLAPSRQDIFQEQLAAIPEFLNIG PLFKSSEPVQLTEAETEYFVRCIKH MFTNHIVFQFDCTNTLNDQLLEKVT VQMEPSDSYEVLSCIPAPSLPYNQP GICYTLVRLPDDDPTAVAGSFSCTM KFTVRDCDPNTGVPDEDGYDDEYVL EDLEVTVSDHIQKVLKPNFAAAWEE VGDTFEKEETFALSSTKTLEEAVNN IITFLGMQPCERSDKVPENKNSHSL YLAGIFRGGYDLLVRSRLALADGVT MQVTVRSKERTPVDVILASVGTRTR PLEQKLISEEDLAANDILDYKDDDD KV |
| 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. |
