C1orf144 抗体 (Alexa Fluor 680)
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- 抗原 See all C1orf144 抗体
- C1orf144 (Chromosome 1 Open Reading Frame 144 (C1orf144))
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适用
- 人, 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
- This C1orf144 antibody is conjugated to Alexa Fluor 680
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C1orf144
- 亚型
- IgG
- Top Product
- Discover our top product C1orf144 Primary Antibody
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anti-Chromosome 1 Open Reading Frame 144 (C1orf144) (N-Term) antibody
C1orf144 适用: 人, 小鼠, 大鼠, 犬, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 1 Open Reading Frame 144 (C1orf144) (N-Term) antibodyC1orf144 适用: 人, 小鼠, 大鼠, Cow, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 1 Open Reading Frame 144 (C1orf144) (AA 6-36), (N-Term) antibodyC1orf144 适用: 人, 小鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 1:50-200
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- C1orf144 (Chromosome 1 Open Reading Frame 144 (C1orf144))
- 别名
- C1orf144 (C1orf144 产品)
- 别名
- MGC82291 antibody, MGC76116 antibody, DKFZp468H135 antibody, C1orf144 antibody, SZRD1 antibody, 1110022I03 antibody, D4Ertd22e antibody, C2H1orf144 antibody, wu:fb15h05 antibody, wu:fk86c07 antibody, zgc:109926 antibody, RGD1560286 antibody, SUZ RNA binding domain containing 1 L homeolog antibody, SUZ RNA binding domain containing 1 antibody, szrd1.L antibody, szrd1 antibody, SZRD1 antibody, Szrd1 antibody
- 背景
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Synonyms: DKFZp566C0424, MGC70432, Putative MAPK-activating protein PM18/PM20/PM22, UPF0485 protein C1orf144, SZRD1_HUMAN, SUZ domain-containing protein 1.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf144 gene product has been provisionally designated C1orf144 pending further characterization.
- 基因ID
- 26099
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