GFAP (phospho S8) polyclonal antibody
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More Files
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Dot Blot (Peptide)
Dot blot analysis of GFAP (phospho S8) polyclonal antibody (Cat # PAB8170) on nitrocellulose membrane. 50 ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.5 ug/mL.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic phosphopeptide of GFAP.
Immunogen
Synthetic phosphopeptide (conjugated with KLH) corresponding to amino acids 1-30 residues surrounding S8 of human GFAP.
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Protein A purification
Recommend Usage
ELISA (1:1000)
Dot Blot (1:500)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Enzyme-linked Immunoabsorbent Assay
Dot Blot (Peptide)
Dot blot analysis of GFAP (phospho S8) polyclonal antibody (Cat # PAB8170) on nitrocellulose membrane. 50 ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.5 ug/mL. -
Gene Info — GFAP
Entrez GeneID
2670Protein Accession#
NP_002046Gene Name
GFAP
Gene Alias
FLJ45472
Gene Description
glial fibrillary acidic protein
Gene Ontology
HyperlinkGene Summary
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq
Other Designations
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Interactome
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Disease
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Publication Reference
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Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.
Shiroma N, Kanazawa N, Kato Z, Shimozawa N, Imamura A, Ito M, Ohtani K, Oka A, Wakabayashi K, Iai M, Sugai K, Sasaki M, Kaga M, Ohta T, Tsujino S.
Brain & Development 2003 Mar; 25(2):116.
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Detection of glial fibrillary acidic protein and neurofilaments in the cerebrospinal fluid of patients with neurocysticercosis.
Quintanar JL, Franco LM, Salinas E.
Parasitology Research 2003 Jul; 90(4):261.
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A new splice variant of glial fibrillary acidic protein, GFAP epsilon, interacts with the presenilin proteins.
Nielsen AL, Holm IE, Johansen M, Bonven B, Jorgensen P, Jorgensen AL.
The Journal of Biological Chemistry 2002 Aug; 277(33):29983.
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Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.
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