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p53 Polyclonal Antibody, 20ul[BT-AP06814] Vacuum Filter Mutations in ADAMTS2 cause Ehlers-Danlos

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p53 Polyclonal Antibody, 20ul[BT-AP06814] Vacuum Filter Mutations in ADAMTS2 cause Ehlers-DanlosTP53 (tumor protein p53) encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in TP53 are associated with a variety of human cancers, including hereditary cancers such as Li Fraumeni

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Description

Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC

eukaryotic translation elongation factor 1 alpha 1 is identified as an autoantigen in 66% of patients with Felty syndrome

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p53 Polyclonal Antibody, 20ul[BT-AP06814] Vacuum Filter Mutations in ADAMTS2 cause Ehlers-DanlosTP53 (tumor protein p53) encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in TP53 are associated with a variety of human cancers, including hereditary cancers such as Li Fraumeni

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