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Protein orgin:

Example: P53_HUMAN, P04637 (UniProt Accession Number), NP_000537, P53 (protein name), Species Summary

If you enter a valid Uniprot ID, UniProt accession number or RefSeq protein ID, the system will not consider the species and reviewed settings of your query. The choices of species and reviewed settings are considered only if you query protein names, protein description or gene names.


Antigenicity Information of Fascin-2

Protein name and sequence of (Fascin-2)

Protein Names
Recommended name:

Fascin-2
Protein IDs
(Accession numbers)
UniProtKB: O14926
NCBI RefSeq: NP_001070650.1
NM_001077182.2
NP_036550.1
NM_012418.3
Organism
Latin Name/
(Common Name) :		 Homo sapiens (Human).
Gene Names FSCN2
Protein Sequence 
    SEQUENCE   492 AA;  55057 MW;  35C85530EF41145C CRC64;
MPTNGLHQVL KIQFGLVNDT DRYLTAESFG FKVNASAPSL KRKQTWVLEP DPGQGTAVLL
RSSHLGRYLS AEEDGRVACE AEQPGRDCRF LVLPQPDGRW VLRSEPHGRF FGGTEDQLSC
FATAVSPAEL WTVHLAIHPQ AHLLSVSRRR YVHLCPREDE MAADGDKPWG VDALLTLIFR
SRRYCLKSCD SRYLRSDGRL VWEPEPRACY TLEFKAGKLA FKDCDGHYLA PVGPAGTLKA
GRNTRPGKDE LFDLEESHPQ VVLVAANHRY VSVRQGVNVS ANQDDELDHE TFLMQIDQET
KKCTFYSSTG GYWTLVTHGG IHATATQVSA NTMFEMEWRG RRVALKASNG RYVCMKKNGQ
LAAISDFVGK DEEFTLKLIN RPILVLRGLD GFVCHHRGSN QLDTNRSVYD VFHLSFSDGA
YRIRGRDGGF WYTGSHGSVC SDGERAEDFV FEFRERGRLA IRARSGKYLR GGASGLLRAD
ADAPAGTALW EY
General annotation
Involvement in disease Defects in FSCN2 are the cause of retinitis pigmentosa type 30 (RP30) [MIM:607921]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP30 inheritance is autosomal dominant.

Suggested Antigen peptide sequence of ( Fascin-2) in rabbit

     

What we offer for Fascin-2

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Detail