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The antibody against GFAP was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 350-432 of human GFAP (NP_002046.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.
The antibody against GFAP was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 350-432 of human GFAP (NP_002046.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.
| Cat.No | ADA-12944A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | gfap |
| Target Synonyms | ALXDRD; GFAP | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.05% proclin300, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Rat brain, Mouse brain | Application | ELISA, WB, IF/ICC, IHC-P |
| Immunogen Description | A synthetic peptide corresponding to a sequence within amino acids 350-432 of human GFAP (NP_002046.1). | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | QDLLNVKLALDIEIATYRKLLEGEENRITIPVQTFSNLQIRETSLDTKSVSEGHLKRNIVVKTVEMRDGEVIKESKQEHKDVM | Uniprot ID | P14136 |
Uniprot Id
P14136
Target Species
Human
Target Name
GFAP
Target Full Name
Glial fibrillary acidic protein
Target Function
GFAP, a class-III intermediate filament, is a cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells.
Target Involvement
Alexander disease (ALXDRD)
Target Subcellular Location
Cytoplasm.
Target Protein Families
Intermediate filament family
Target Tissue Specificity
Expressed in cells lacking fibronectin.
Target Research Area
Neuroscience
Target Synonyms
ALXDRD; GFAP
Target Background
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.
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