CTDSPL2 抗体 (AA 11-110) (AbBy Fluor® 555)
Quick Overview for CTDSPL2 抗体 (AA 11-110) (AbBy Fluor® 555) (ABIN1398017)
抗原
See all CTDSPL2 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 11-110
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交叉反应
- 人
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预测反应
- Mouse,Rat,Dog,Sheep,Horse
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human CTDSPL2
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亚型
- IgG
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anti-CTD (Carboxy-Terminal Domain, RNA Polymerase II, Polypeptide A) Small Phosphatase Like 2 (CTDSPL2) (AA 52-80), (N-Term) antibody
CTDSPL2 适用: 人, 小鼠 WB, FACS 宿主: 兔 Polyclonal RB30136 unconjugated
anti-CTD (Carboxy-Terminal Domain, RNA Polymerase II, Polypeptide A) Small Phosphatase Like 2 (CTDSPL2) (AA 55-84), (N-Term) antibodyCTDSPL2 适用: 人, 小鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
anti-CTD (Carboxy-Terminal Domain, RNA Polymerase II, Polypeptide A) Small Phosphatase Like 2 (CTDSPL2) (AA 11-110) antibodyCTDSPL2 适用: 人 WB, ELISA, IF (cc), IF (p), IHC (fro), IHC (p) 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
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- CTDSPL2 (CTD (Carboxy-Terminal Domain, RNA Polymerase II, Polypeptide A) Small Phosphatase Like 2 (CTDSPL2))
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别名
- CTDSPL2
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背景
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Synonyms: CTD small phosphatase like protein 2, CTD small phosphatase-like protein 2, CTDSP like 2, CTDSP-like 2, ctdspl2, CTSL2_HUMAN, HSPC058, HSPC129.
Background: CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
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基因ID
- 51496
抗原
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