MOXD1 抗体 (AA 501-600) (Biotin)
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- 抗原 See all MOXD1 抗体
- MOXD1 (Monooxygenase, DBH-Like 1 (MOXD1))
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抗原表位
- AA 501-600
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适用
- 人, 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 MOXD1 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
- 人, 小鼠
- 预测反应
- Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human MOXD1
- 亚型
- IgG
- Top Product
- Discover our top product MOXD1 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
- MOXD1 (Monooxygenase, DBH-Like 1 (MOXD1))
- 别名
- MOXD1 (MOXD1 产品)
- 别名
- MOX antibody, PRO5780 antibody, dJ248E1.1 antibody, 3230402N08Rik antibody, MNCb-5203 antibody, DBHR antibody, monooxygenase, DBH-like 1 antibody, monooxygenase DBH like 1 antibody, Moxd1 antibody, MOXD1 antibody
- 背景
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Synonyms: DBH like monooxygenase protein 1, DBH-like monooxygenase protein 1, dJ248E1.1, DKFZp564G202, Monooxygenase X, monooxygenase, DBH like 1, MOX, Moxd1, MOXD1_HUMAN, PRO5780.
Background: MOXD1 is a 613 amino acid single-pass type I membrane protein of the Endoplasmic reticulum that belongs to the copper type II ascorbate-dependent monooxygenase family. Existing as two alternatively spliced isoforms, MOXD1 is expressed in adult spinal cord, adrenal gland, brain, testis, uterus, lung and kidney, as well as fetal liver and brain. MOXD1 is upregulated during replicative senescence in primary fibroblast and umbilical vein endothelial cell cultures, and uses two copper ions per subunit as a cofactor. MOXD1 contains one DOMON domain, undergoes post-translational N-glycosylation and is encoded by a gene that maps to human chromosome 6. Chromosome 6 contains 170 million base pairs, comprises nearly 6 % of the human genome and is associated with early onset intestinal cancer, Porphyria cutanea tarda, Parkinson's disease and Stickler syndrome.
- 基因ID
- 26002
- UniProt
- Q6UVY6
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