This gene encodes a muscle-specific small heat shock protein. A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C.[provided by RefSeq, Sep 2010].
custom-made
HSPB3
Origine: Humain
Hôte: HEK-293 Cells
Recombinant
> 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
custom-made
HSPB3
Origine: Souris
Hôte: HEK-293 Cells
Recombinant
> 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
custom-made
HSPB3
Origine: Souris
Hôte: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
SDS, WB, ELISA
custom-made
HSPB3
Origine: Humain
Hôte: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
SDS, WB, ELISA
heat shock protein family B (small) member 3 (HSPB3) Protéines heat shock 27kDa protein 3 (HSPB3) Protéines heat shock protein family B (small) member 3 (hspb3) Protéines heat shock protein family B (small) member 3 (Hspb3) Protéines heat shock protein 3 (Hspb3) Protéines 2310035K17Rik Protéines AI844863 Protéines DHMN2C Protéines HMN2C Protéines Hsbp3 Protéines HSPB3 Protéines HSPL27 Protéines spb3 Protéines