DPY19L1 抗体 (AA 571-675) (Biotin)
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- 抗原 See all DPY19L1 抗体
- DPY19L1 (Dpy-19-Like 1 (C. Elegans) (DPY19L1))
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抗原表位
- AA 571-675
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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 DPY19L1 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,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit,Zebrafish
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DPY19L1
- 亚型
- IgG
- Top Product
- Discover our top product DPY19L1 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
- DPY19L1 (Dpy-19-Like 1 (C. Elegans) (DPY19L1))
- 别名
- DPY19L1 (DPY19L1 产品)
- 别名
- 1100001I19Rik antibody, 6030402K12 antibody, AI225861 antibody, AW558481 antibody, RGD1305822 antibody, dpy-19 like C-mannosyltransferase 1 antibody, probable C-mannosyltransferase DPY19L1 antibody, dpy-19 like 1 antibody, dpy-19-like 1 (C. elegans) antibody, DPY19L1 antibody, LOC100011919 antibody, dpy19l1 antibody, Dpy19l1 antibody
- 背景
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Synonyms: D19L1_HUMAN, Dpy 19 like 1 C. elegans, Dpy 19 like protein 1, Dpy-19-like protein 1, DPY19L1, GA0500, KIAA0877, Protein dpy 19 homolog 1, Protein dpy-19 homolog 1, Protein dpy19 homolog 1.
Background: Dpy-19 (dumpy-19), is a 683 amino acid C. elegans protein that is required to orient the neuroblasts QL and QR correctly on the anterior/posterior axis. Dpy-19 is expressed highly in dorsal hyp7 cells, ventral P cells and lateral V cells, and dorsal and ventral body muscle cells. DPY19L1 (Dpy-19-like protein 1), also known as KIAA0877, is a 675 amino acid multi-pass membrane protein that belongs to the Dpy-19 family. DPY19L1 is expressed as two isoforms produced by alternative splicing and is encoded by a gene mapping to human chromosome 7, which encodes over 1,000 genes and makes up about 5 % of the human genome. Diseases associated with chromosome 7 include Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
- 基因ID
- 23333
- 途径
- SARS-CoV-2 Protein Interactome
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