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Mutations in this gene cause Bardet-Biedl syndrome type 10
Catalogue Numbers: BS71337-50
GPRC6A Polyclonal Antibody
Background: Polymerase Chain Reaction (PCR)
Extra Notes: Immunohistochemistry (IHC) analyzes of Laminin γ-3 (T1385) pAb in paraffin-embedded human breast carcinoma tissue at 1:50
Cox-17 (N8) Polyclonal Antibody-BS2514 Size:100µl Mutations in this gene causeCox 17 (N8) Polyclonal Antibody Product: Rabbit IgG, 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Catalogue Numbers: BS2514 50, BS2514 100 Sizes: 50l, 100l Swiss Prot: Q14061 Host: Rabbit Reactivity: Human Applications: WB, IHC, IF Background: Cytochrome c oxidase 17 (COX17) is a nuclear gene encoding an assembly protein necessary for proper COX apoenzyme dependent mitochondrial respiration. The mammalian COX apoenzyme is a heteromer
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