CNOT11 抗体 (Cy5.5)
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- 抗原 See all CNOT11 抗体
- CNOT11 (CCR4-NOT Transcription Complex, Subunit 11 (CNOT11))
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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 CNOT11 antibody is conjugated to Cy5.5
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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 C2orf29
- 亚型
- IgG
- Top Product
- Discover our top product CNOT11 Primary Antibody
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anti-CCR4-NOT Transcription Complex, Subunit 11 (CNOT11) (AA 143-192) antibody
CNOT11 适用: 人, 小鼠, 大鼠, Cow, 犬, Pig, 猴, Bat, Hamster WB 宿主: 兔 Polyclonal unconjugated
anti-CCR4-NOT Transcription Complex, Subunit 11 (CNOT11) (AA 215-264) antibodyCNOT11 适用: 人, 小鼠, 大鼠, Cow, 犬, Pig, 斑马鱼, 豚鼠, 马, 兔, 猴, Bat, Hamster, 非洲爪蟾, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-CCR4-NOT Transcription Complex, Subunit 11 (CNOT11) (N-Term) antibodyCNOT11 适用: 人 WB 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
- CNOT11 (CCR4-NOT Transcription Complex, Subunit 11 (CNOT11))
- 别名
- C2orf29 (CNOT11 产品)
- 别名
- C2orf29 antibody, 2410015L18Rik antibody, C40 antibody, D1Bwg0212e antibody, RGD1560909 antibody, fj49e01 antibody, wu:fj49e01 antibody, zgc:163002 antibody, CCR4-NOT transcription complex subunit 11 antibody, CCR4-NOT transcription complex, subunit 11 antibody, CNOT11 antibody, Cnot11 antibody, cnot11 antibody
- 背景
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Synonyms: C2orf29, C40, CB029_HUMAN, Chromosome 2 open reading frame 29, Hypothetical protein LOC55571, UPF0760 protein C2orf29.
Background: C2orf29, also known as C40, is a 510 amino acid protein that belongs to the UPF0760 family and is encoded by a gene that maps to human chromosome 2q11.2. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
- 基因ID
- 55571
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