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AFG3L2 Polyclonal Antibody, 50ul Cellular Function Assays ground-breaking experiments

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AFG3L2 Polyclonal Antibody, 50ul Cellular Function Assays ground-breaking experimentsThis gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

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Description

ground-breaking experiments

NF-κB-activating agents can induce the phosphorylation of IκB proteins

ready-to-use solution for efficient protein digestion

Contains 4 EF-hand domains

400 genes and comprises nearly 4% of the human genome

AFG3L2 Polyclonal Antibody, 50ul Cellular Function Assays ground-breaking experimentsThis gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

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