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Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13)
genus Orthohantavirus) are RNA viruses transmitted by aerosolized excreta from infected rodents and shrews
Belonging to the FNDC3 family of proteins
The OTU subfamily comprises a group of approximately 100 putative cysteine proteases that are homologous to the ovarian tumor gene product of Drosophila
Specificity: CXCL17 Antibody detects endogenous levels of total CXCL17
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),
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