C11orf46 抗体 (Cy5)
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- 抗原 See all C11orf46 抗体
- C11orf46 (Chromosome 11 Open Reading Frame 46 (C11orf46))
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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 C11orf46 antibody is conjugated to Cy5
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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 C11ORF46
- 亚型
- IgG
- Top Product
- Discover our top product C11orf46 Primary Antibody
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anti-Chromosome 11 Open Reading Frame 46 (C11orf46) (AA 35-84) antibody
C11orf46 适用: 人, 小鼠, 豚鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 11 Open Reading Frame 46 (C11orf46) (N-Term) antibodyC11orf46 适用: 人, 小鼠, 大鼠, 豚鼠, 兔, Cow, 犬, 马 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
- C11orf46 (Chromosome 11 Open Reading Frame 46 (C11orf46))
- 别名
- C11ORF46 (C11orf46 产品)
- 别名
- MGC115732 antibody, ARF7EP antibody, C11orf46 antibody, dJ299F11.1 antibody, 2700007P21Rik antibody, 4930448O08Rik antibody, RGD1311463 antibody, C15H11orf46 antibody, ARL14EP antibody, ADP ribosylation factor like GTPase 14 effector protein L homeolog antibody, ADP ribosylation factor like GTPase 14 effector protein antibody, ADP-ribosylation factor-like 14 effector protein antibody, ADP-ribosylation factor like GTPase 14 effector protein antibody, arl14ep.L antibody, arl14ep antibody, ARL14EP antibody, Arl14ep antibody
- 背景
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Synonyms: Chromosome 11 open reading frame 46, DJ299F11.1, FLJ38968, Hypothetical protein LOC120534, Uncharacterized protein C11orf46, AL14E_HUMAN.
Background: C11orf46, also known as FLJ38968 or dJ299F11.1, is a 260 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
- 基因ID
- 120534
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