Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13)
Catalogue Numbers: BS71681-50
RRID: AB_2840503
Belonging to the FNDC3 family of proteins
Catalogue Numbers: DF10279-100
Recombinant Human CD20/MS4A1 Protein (aa 213-297, His Tag) - PKSH031312 Magnetic Separation Rack Defects in HSPD1 are aRecombinant Human CD20 MS4A1 Protein (aa 213 297, His Tag) Size: 20g Catalogue Number: PKSH031312 20 Citations, Manuals and MSDS Available upon request. Abbreviation: CD20, MS4A1 Target Synonym: B1, Bp35, CD20, CVID5, LEU 16, MS4A1, MS4A2, S7 Research Areas: Cancer, immunology, Stem cells Target Species: Human Expression Host: HEK293 Cells Fusion Tag: N His Accession: NP_068769. 2 Background: CD20 (membrane spanning 4 domains, subfamily A, member 1),