GLB1L3 抗体 (AA 51-150) (Biotin)
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- 抗原 See all GLB1L3 products
- GLB1L3 (Galactosidase, beta 1-Like 3 (GLB1L3))
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抗原表位
- AA 51-150
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适用
- 小鼠
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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 GLB1L3 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))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GLB1L3
- 亚型
- IgG
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anti-Galactosidase, beta 1-Like 3 (GLB1L3) (AA 1-236) antibody
GLB1L3 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Galactosidase, beta 1-Like 3 (GLB1L3) antibodyGLB1L3 适用: 人, 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
anti-Galactosidase, beta 1-Like 3 (GLB1L3) (AA 1-313) antibodyGLB1L3 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Galactosidase, beta 1-Like 3 (GLB1L3) (AA 180-290) antibodyGLB1L3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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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
- GLB1L3 (Galactosidase, beta 1-Like 3 (GLB1L3))
- 别名
- GLB1L3 (GLB1L3 产品)
- 别名
- 4921509F24Rik antibody, GLB1L3 antibody, galactosidase, beta 1 like 3 antibody, galactosidase beta 1 like 2 antibody, galactosidase beta 1 like 3 antibody, galactosidase, beta 1-like 3 antibody, Glb1l3 antibody, GLB1L2 antibody, GLB1L3 antibody
- 背景
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Synonyms: Beta galactosidase 1 like protein 3, Beta-galactosidase-1-like protein 3, FLJ90231, Galactosidase, beta 1 like 3, GLB1L 3, Glb1l3, GLBL3_HUMAN, LOC112937, OTTHUMP00000235427.
Background: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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