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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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: GFAP; Glial fibrillary acidic protein; glial fibrillary acidic protein alpha; intermediate filament; intermediate filament protein
Gene Aliases: AI836096; ALXDRD; GFAP
UniProt ID: (Human) P14136, (Rat) P47819, (Mouse) P03995
Entrez Gene ID: (Human) 2670, (Rat) 24387, (Mouse) 14580
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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