FITC标记的γ氨基丁酸转氨酶抗体
产品名称： FITC标记的γ氨基丁酸转氨酶抗体
英文名称： Anti-ABAT/FITC
产品编号： HZ-4234R-FITC
产品价格： null
产品产地： 中国/上海
品牌商标： HZbscience
更新时间： 2023-08-17T10:24:20
使用范围： IF=1:50-200
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Rabbit Anti-ABAT/FITC Conjugated antibody
FITC标记的γ氨基丁酸转氨酶抗体
| 英文名称 | Anti-ABAT/FITC |
| 中文名称 | FITC标记的γ氨基丁酸转氨酶抗体 |
| 别 名 | mitochondrial; (S) 3 amino 2 methylpropionate transaminase; (S)-3-amino-2-methylpropionate transaminase; 4 aminobutyrate aminotransferase; 4 aminobutyrate aminotransferase, mitochondrial; 4-aminobutyrate aminotransferase; ABAT; GABA aminotransferase; GABA AT; GABA T; GABA transaminase; GABA transferase; GABA-AT; GABA-T; GABAT; GABT_HUMAN; Gamma amino N butyrate transaminase; Gamma-amino-N-butyrate transaminase; L AIBAT; L-AIBAT; LAIBAT. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 肿瘤 免疫学 神经生物学 信号转导 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Rat, Pig, Cow, Horse, |
| 产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 56kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human ABAT |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| 产品介绍 | background: Catalyzes the conversion of gamma-aminobutyrate and L-beta-aminoisobutyrate to succinate semialdehyde and methylmalonate semialdehyde, respectively. Can also convert delta-aminovalerate and beta-alanine. Function: Catalyzes the conversion of gamma-aminobutyrate and L-beta-aminoisobutyrate to succinate semialdehyde and methylmalonate semialdehyde, respectively. Can also convert delta-aminovalerate and beta-alanine. Subunit: Homodimer; disulfide-linked. Subcellular Location: Mitochondrion matrix. Tissue Specificity: Liver > pancreas > brain > kidney > heart > placenta. DISEASE: Defects in ABAT are a cause of gamma-aminobutyrate transaminase deficiency (GABA-AT deficiency) [MIM:613163]. The phenotype of this deficiency includes psychomotor retardation, hypotonia, hyperreflexia, lethargy, refractory seizures, and EEG abnormalities. Similarity: Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. Database links: Entrez Gene: 18 Human Entrez Gene: 268860 Mouse Entrez Gene: 81632 Rat Omim: 137150 Human SwissProt: P80404 Human SwissProt: P61922 Mouse SwissProt: P50554 Rat Unigene: 336768 Human Unigene: 259315 Mouse Unigene: 10090 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
催化γ-氨基丁酸和L-β-氨基异丁酸酯转化为琥珀酸半醛和甲基丙二酸半醛。还可以转化δ氨基戊酸酯和β-丙氨酸。