Human CTSA (Cathepsin A) ELISA Kit - RE2693H Affinity Biosciences Mutations in this gene cause

Mutations in this gene cause the autosomal dominant disorder

Alternative Name: GSDMA

RRID: AB_2837249

lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts

Swiss-Prot: P01148

Human CTSA (Cathepsin A) ELISA Kit - RE2693H Affinity Biosciences Mutations in this gene causeHuman CTSA (Cathepsin A) ELISA Kit Sizes: 48T, 96T Catalogue Numbers: RE2693H 48, RE2693H 96 Citations, Manuals and MSDS Available upon request. Species: Human Alternative Names: CTSA, GLB2, GSL, NGBE, PPCA, PPGB, cathepsin A Detection method: Sandwich Reaction time: 3. 5H Research Areas: Cytokine; Sensitivity: 46. 88 pg mL Detection Range: 78. 13 5000pg mL Sample Types: Serum, Plasma, Tissue homogenate and Other biological samples; Sample Volume=100L