C12ORF23 抗体 (PE)
This 兔 多克隆 antibody specifically detects C12ORF23 in FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN1431916
发货至:
中国
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Quick Overview for C12ORF23 抗体 (PE) (ABIN1431916)
抗原
C12ORF23
(Chromosome 12 Open Reading Frame 23 (C12ORF23))
适用
人, 小鼠, 大鼠
宿主
兔
克隆类型
多克隆
标记
This C12ORF23 antibody is conjugated to PE
应用范围
Flow Cytometry (FACS)
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human C12orf23
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亚型
- IgG
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应用备注
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FCM: (1:20-100)
Optimal working dilution should be determined by the investigator. -
说明
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Exitation/Emission: 480,565nm/578nm
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 100 μg/mL BSA, 50 % glycerol and 0.09 % sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at 4 °C for 12 months.
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有效期
- 12 months
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- C12ORF23 (Chromosome 12 Open Reading Frame 23 (C12ORF23))
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别名
- C12orf23
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背景
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C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a number of skeletal deformities, 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.
Synonyms: C12orf23, Chromosome 12 open reading frame 23, CL023_HUMAN, MGC17943, UPF0444 transmembrane protein C12orf23. -
基因ID
- 90488
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HGNC
- 0
抗原
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