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Defects in HPGD are the cause of primary hypertrophic osteoathropathy autosomal recessive (PHOAR)
Specificity: Recognizes endogenous levels of Cathepsin Z protein
where it binds to hydroxyapatite in a calcium-dependent manner
E-AB-19926-120
TMEM132D Polyclonal Antibody - E-AB-91455 Creative BioMart Defects in HPGD are theTMEM132D Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 91455 60, E AB 91455 120, E AB 91455 200 Citations, Manuals and MSDS Available upon request. Abbreviation: TMEM132D Target Synonym: TMEM132D; MOLT; PPP1R153 Conjugation: Unconjugated Host: Rabbit Species Reactivity: Human, Mouse, Rat Application: WB Isotype: IgG Clonality: Polyclonal UNIProt ID: Q14C87 Background: May serve as a cell surface marker for oligodendrocyte