C12ORF29 抗体 (Alexa Fluor 594)
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- 抗原 See all C12ORF29 products
- C12ORF29 (Chromosome 12 Open Reading Frame 29 (C12ORF29))
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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 C12ORF29 antibody is conjugated to Alexa Fluor 594
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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 C12ORF29
- 亚型
- IgG
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anti-Chromosome 12 Open Reading Frame 29 (C12ORF29) (AA 61-89), (N-Term) antibody
C12ORF29 适用: 人, 小鼠 WB, FACS, IF, IHC (p) 宿主: 兔 Polyclonal RB28694 unconjugated
anti-Chromosome 12 Open Reading Frame 29 (C12ORF29) (AA 68-96), (N-Term) antibodyC12ORF29 适用: 人, 小鼠 WB, FACS, IF, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 29 (C12ORF29) (AA 30-43) antibodyVerified C12ORF29 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 29 (C12ORF29) (AA 1-325) antibodyC12ORF29 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
- C12ORF29 (Chromosome 12 Open Reading Frame 29 (C12ORF29))
- 别名
- C12ORF29 (C12ORF29 产品)
- 别名
- C12orf29 antibody, 4930571E09Rik antibody, A730088G13Rik antibody, AW551239 antibody, C430008C19Rik antibody, chromosome 12 open reading frame 29 antibody, chromosome 5 open reading frame, human C12orf29 antibody, chromosome 3 open reading frame, human C12orf29 antibody, RIKEN cDNA 4930430F08 gene antibody, C12orf29 antibody, C5H12orf29 antibody, C3H12orf29 antibody, 4930430F08Rik antibody
- 背景
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Synonyms: CL029_HUMAN, Uncharacterized protein C12orf29.
Background: 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 varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf29 gene product has been provisionally designated C12orf29 pending further characterization.
- 基因ID
- 91298
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