GBAS 抗体 (AA 21-120) (Biotin)
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- 抗原 See all GBAS 抗体
- GBAS (Glioblastoma Amplified Sequence (GBAS))
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抗原表位
- AA 21-120
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This GBAS antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GBAS
- 亚型
- IgG
- Top Product
- Discover our top product GBAS Primary Antibody
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- GBAS (Glioblastoma Amplified Sequence (GBAS))
- 别名
- GBAS (GBAS 产品)
- 别名
- nipsnap2 antibody, wu:fc08b08 antibody, zgc:92497 antibody, NIPSNAP2 antibody, AV006093 antibody, Nipsnap2 antibody, nipsnap homolog 2 antibody, glioblastoma amplified sequence antibody, nipsnap2 antibody, NIPSNAP2 antibody, GBAS antibody, Nipsnap2 antibody
- 背景
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Synonyms: 4 nitrophenylphosphatase domain and non neuronal SNAP25 like 2, gbas, Glioblastoma amplied sequence, Glioblastoma-amplied sequence, NIPS2_HUMAN, Nipsnap homolog 2, NipSnap2, Protein NipSnap homolog 2.
Background: NIPSNAP2 is a 286 amino acid protein that is abundantly expressed in heart and skeletal muscle. Belonging to the NIPSNAP family, NIPSNAP2 may be involved in vesicular transport. NIPSNAP2 contains a signal peptide, a transmembrane domain and two tyrosine phosphorylation sites. NIPSNAP2 is encoded by a gene mapping to human chromosome 7p11.2. Chromosomal region 7p12 is amplified in approximately 40 % of glioblastomas, the most common and malignant form of central nervous system tumor. Human chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.
- 基因ID
- 2631
- 途径
- Ribonucleoside Biosynthetic Process
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