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For maximum recovery of product, centrifuge the vial prior to removing the cap.
Sequence of this protein is as follows: KTVEMRDGEV IK
GFAP (R416W) refers to a specific mutation in the GFAP gene, where arginine (R) at position 416 is substituted with tryptophan (W). GFAP, or Glial Fibrillary Acidic Protein, is an intermediate filament protein expressed in astrocytes, providing structural support to these glial cells in the central nervous system. The R416W mutation is associated with Alexander disease, a rare neurodegenerative disorder characterized by the accumulation of GFAP aggregates, leading to astrocyte dysfunction and progressive neurological impairment.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: GFAP; Glial fibrillary acidic protein; glial fibrillary acidic protein alpha; intermediate filament; intermediate filament protein
基因别名: AI836096; ALXDRD; GFAP
UniProt ID: (Human) P14136, (Rat) P47819, (Mouse) P03995
Entrez Gene ID: (Human) 2670, (Rat) 24387, (Mouse) 14580