C12orf4 抗体
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- 抗原 See all C12orf4 products
- C12orf4 (Chromosome 12 Open Reading Frame 4 (C12orf4))
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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 C12orf4 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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 C12ORF4
- 亚型
- IgG
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anti-Chromosome 12 Open Reading Frame 4 (C12orf4) (AA 179-228) antibody
C12orf4 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 马, 豚鼠, 猴, Bat, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 4 (C12orf4) (AA 71-120) antibodyC12orf4 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 马, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 4 (C12orf4) (N-Term) antibodyC12orf4 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- C12orf4 (Chromosome 12 Open Reading Frame 4 (C12orf4))
- 别名
- C12ORF4 (C12orf4 产品)
- 别名
- MGC53313 antibody, C12orf4 antibody, MGC79726 antibody, chromosome 12 open reading frame 4 L homeolog antibody, chromosome 1 open reading frame, human C12orf4 antibody, chromosome 12 open reading frame 4 antibody, chromosome 11 open reading frame, human C12orf4 antibody, chromosome 12 open reading frame, human C12orf4 antibody, DNA segment, Chr 6, Wayne State University 163, expressed antibody, c12orf4.L antibody, C1H12ORF4 antibody, c12orf4 antibody, C11H12orf4 antibody, C12H12orf4 antibody, C12orf4 antibody, D6Wsu163e antibody
- 背景
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Synonyms: chromosome 12 open reading frame 4, FLJ21158, FLJ23899, hypothetical protein LOC57102, CL004_HUMAN.
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 C12orf4 gene product has been provisionally designated C12orf4 pending further characterization.
- 基因ID
- 57102
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