C1ORF216 抗体 (AA 101-200) (Alexa Fluor 350)
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- 抗原 See all C1ORF216 products
- C1ORF216 (Chromosome 1 Open Reading Frame 216 (C1ORF216))
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抗原表位
- AA 101-200
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适用
- 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 C1ORF216 antibody is conjugated to Alexa Fluor 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse,Dog,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C1orf216
- 亚型
- IgG
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anti-Chromosome 1 Open Reading Frame 216 (C1ORF216) (C-Term) antibody
C1ORF216 适用: 大鼠, 人, 小鼠, Cow, 犬, 猴, Bat, 小鸡, Hamster, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 1 Open Reading Frame 216 (C1ORF216) (AA 51-100) antibodyC1ORF216 适用: 大鼠, 人, 小鼠, 马, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 1 Open Reading Frame 216 (C1ORF216) antibodyC1ORF216 适用: 人 IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 1 Open Reading Frame 216 (C1ORF216) (N-Term) antibodyC1ORF216 适用: 大鼠, 人, 小鼠, 马, Cow, 豚鼠 WB 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
- 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
- C1ORF216 (Chromosome 1 Open Reading Frame 216 (C1ORF216))
- 别名
- C1orf216 (C1ORF216 产品)
- 别名
- 7530403E16Rik antibody, AI849033 antibody, RIKEN cDNA 5730409E04Rik gene antibody, chromosome 1 open reading frame 216 antibody, chromosome 1 open reading frame 216 S homeolog antibody, 5730409E04Rik antibody, C1orf216 antibody, c1orf216.S antibody
- 背景
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Synonyms: 5730409E04Rik, C1orf216, CA216_HUMAN, chromosome 1 open reading frame 216, hypothetical protein LOC127703, UPF0500 protein C1orf216.
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 C1orf216 gene product has been provisionally designated C1orf216 pending further characterization.
- 基因ID
- 127703
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