SBNO1 抗体 (AA 331-430) (Alexa Fluor 555)
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- 抗原 See all SBNO1 抗体
- SBNO1 (Strawberry Notch Homolog 1 (SBNO1))
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抗原表位
- AA 331-430
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适用
- 人
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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 SBNO1 antibody is conjugated to Alexa Fluor 555
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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
- 人
- 预测反应
- Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit,Zebrafish
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SBNO1
- 亚型
- IgG
- Top Product
- Discover our top product SBNO1 Primary Antibody
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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
- SBNO1 (Strawberry Notch Homolog 1 (SBNO1))
- 别名
- SBNO1 (SBNO1 产品)
- 别名
- 9330180L10Rik antibody, AI849128 antibody, AW557836 antibody, BC021875 antibody, Sbno antibody, mSno1 antibody, sno antibody, MOP3 antibody, Sno antibody, strawberry notch homolog 1 (Drosophila) antibody, strawberry notch homolog 1 antibody, microRNA 8072 antibody, Sbno1 antibody, SBNO1 antibody, MIR8072 antibody
- 背景
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Synonyms: FLJ10701, FLJ10833, FLJ16176, Monocyte protein 3, MOP 3, MOP-3, MOP3, Protein strawberry notch homolog 1, SBNO 1, Sbno1, SBNO1_HUMAN, Sno, Sno strawberry notch homolog 1, Strawberry notch homolog 1.
Background: SBNO1 is a 1,392 amino acid protein encoded by the human gene of the same name located on chromosome 12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster, encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms which vary in severity depending on the extent of mosaicism. It is most severe in cases of complete trisomy.
- 基因ID
- 55206
- UniProt
- A3KN83
- 途径
- SARS-CoV-2 Protein Interactome
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