Chromosome 15 Open Reading Frame 58 (C15orf58) (AA 301-385) 抗体 (HRP)
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- 抗原 See all Chromosome 15 Open Reading Frame 58 (C15orf58) 抗体
- Chromosome 15 Open Reading Frame 58 (C15orf58)
- 抗原表位
- AA 301-385
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适用
- 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- HRP
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 小鼠, 大鼠
- 预测反应
- Human,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58
- 亚型
- IgG
- Top Product
- Discover our top product C15orf58 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.
- 注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- 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
- Chromosome 15 Open Reading Frame 58 (C15orf58)
- 别名
- GDPGP1/C15orf58 (C15orf58 产品)
- 别名
- C15orf58 antibody, VTC2 antibody, D330012F22Rik antibody, C21H15orf58 antibody, c15orf58 antibody, GDP-D-glucose phosphorylase 1 antibody, GDP-D-glucose phosphorylase 1 S homeolog antibody, GDPGP1 antibody, Gdpgp1 antibody, gdpgp1.S antibody
- 背景
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Synonyms: C15orf58, Chromosome 15 open reading frame 58, GDP-D-glucose phosphorylase 1, GDP-D-glucose phosphorylase C15orf58, gdpgp1, GDPP1_HUMAN, VTC2.
Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
- 基因ID
- 390637
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