GLYATL1 抗体 (AA 101-200) (FITC)
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- 抗原 See all GLYATL1 抗体
- GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))
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抗原表位
- AA 101-200
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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 GLYATL1 antibody is conjugated to FITC
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GLYATL1
- 亚型
- IgG
- Top Product
- Discover our top product GLYATL1 Primary Antibody
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anti-Glycine-N-Acyltransferase-Like 1 (GLYATL1) antibody
GLYATL1 适用: 人 WB, IHC (p), ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Glycine-N-Acyltransferase-Like 1 (GLYATL1) (AA 1-302) antibodyGLYATL1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glycine-N-Acyltransferase-Like 1 (GLYATL1) (AA 73-302) antibodyGLYATL1 适用: 人 WB, IHC, IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))
- 别名
- GLYATL1 (GLYATL1 产品)
- 别名
- GATF-C antibody, GNAT antibody, glycine-N-acyltransferase like 1 antibody, GLYATL1 antibody
- 背景
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Synonyms: Acyl CoA glycine N acyltransferase like protein 1, EC 2.3.1.13, FLJ26507, FLJ34646, GATF C, GATFC, Glycine N acyltransferase like 1, GNAT, MGC15397, MGC15937, GLYL1_HUMAN.
Background: GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
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