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autosomal recessive craniometaphyseal dysplasia and heart malformations
Catalogue Numbers: BS5899-50
Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome
Catalogue Numbers: E-UNEL-H0120-96Tx15
Cross Reactivity: This kit recognizes Human MT1E in samples
NOP58 Polyclonal Antibody-BS78588 Size:50µl autosomal recessive craniometaphyseal dysplasia andNOP58 Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS78588 50, BS78588 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q9Y2X3 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IF ICC All Applications: WB,1: 500 1: 2000 IF ICC,1: 50 1: 200 Background: The protein encoded by this gene is a core component of box C D small nucleolar ribonucleoproteins. Some box C D small nucleolar RNAs (snoRNAs),
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