Anti-GFAP Mouse Monoclonal Antibody (CAB11864)
- SKU:
- CAB11864
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Mouse
- Isotype:
- IgG
- Antibody Type:
- Monoclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
抗体名: | Anti-GFAP Mouse Monoclonal Antibody |
抗体コード: | CAB11864 |
抗体サイズ: | 50 uL |
申し込み: | WB IHC IF |
反応性: | Human, Mouse, Rat |
宿主種: | Mouse |
免疫原: | Recombinant protein of human GFAP |
申し込み: | WB IHC IF |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:100 IF 1:50 - 1:100 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | Mouse brain, Rat brain |
免疫原: | Recombinant protein of human GFAP |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | Email for sequence |
遺伝子ID: | 2670 |
Uniprot: | P14136 |
セルラーロケーション: | Cytoplasm |
計算された分子量: | 49kDa/50kDa |
観察された分子量: | 50kDa |
同義語: | ALXDRD, GFAP |
バックグラウンド: | 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. |
UniProt Protein Function: | GFAP: a class-III intermediate filament protein. A cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant isoform has been described, but its full length sequence has not been determined. |
UniProt Protein Details: | Protein type:Cytoskeletal Chromosomal Location of Human Ortholog: 17q21 Cellular Component: membrane; cytoplasm; intermediate filament; cytosol Molecular Function:integrin binding; structural constituent of cytoskeleton; kinase binding Biological Process: Bergmann glial cell differentiation; extracellular matrix organization and biogenesis; regulation of neurotransmitter uptake; response to wounding; intermediate filament organization; neurite regeneration; astrocyte development Disease: Alexander Disease |
NCBI 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, Oct 2008] |
UniProt Code: | P14136 |
NCBI GenInfo Identifier: | 121135 |
NCBI Gene ID: | 2670 |
NCBI Accession: | P14136.1 |
UniProt Secondary Accession: | P14136,Q53H98, Q5D055, Q6ZQS3, Q7Z5J6, Q7Z5J7, Q96KS4 Q96P18, Q9UFD0, B2RD44, D3DX59, E9PAX3, |
UniProt Related Accession: | P14136 |
Molecular Weight: | 432 |
NCBI Full Name: | Glial fibrillary acidic protein |
NCBI Synonym Full Names: | glial fibrillary acidic protein |
NCBI Official Symbol: | GFAP |
NCBI Protein Information: | glial fibrillary acidic protein |
UniProt Protein Name: | Glial fibrillary acidic protein |
Protein Family: | Glial fibrillary acidic protein |
UniProt Gene Name: | GFAP |
UniProt Entry Name: | GFAP_HUMAN |