GFAP (phospho S8) Peptide
产品名称： GFAP (phospho S8) Peptide
英文名称： GFAP (phospho S8) Peptide
产品编号： P1691
产品价格： 0
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围： null
亚诺法生技股份有限公司（Abnova)
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- 邮编 : 11493
- 所在区域 : 台湾
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- 邮箱 : sales@abnova.com.tw
- 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
- 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.
- Recommend Usage:
- ELISA (1:1000)
Dot Blot (1:500)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Publication Reference
- 1.
- 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 Dev. 2003 Mar;25(2):116-21.
- 2.
- Detection of glial fibrillary acidic protein and neurofilaments in the cerebrospinal fluid of patients with neurocysticercosis.
Quintanar JL, Franco LM, Salinas E.Parasitol Res. 2003 Jul;90(4):261-3. Epub 2003 Mar 12.
- 3.
- 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.J Biol Chem. 2002 Aug 16;277(33):29983-91. Epub 2002 Jun 10.
- Entrez GeneID:
- 2670
- Protein Accession#:
- NP_002046
- Gene Name:
- GFAP
- Gene Alias:
- FLJ45472
- Gene Description:
- glial fibrillary acidic protein
- Gene Ontology:
- Hyperlink
- Gene 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:
- -
- Related Disease