PUS7L 抗体 (AA 165-699)
This 兔 多克隆 antibody specifically detects PUS7L in WB, ELISA, IF 和 IHC (p). It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7871150
发货至:
中国
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Quick Overview for PUS7L 抗体 (AA 165-699) (ABIN7871150)
抗原
PUS7L
(Pseudouridylate Synthase 7 Homolog-Like (PUS7L))
适用
人, 小鼠, 大鼠
宿主
兔
克隆类型
多克隆
标记
This PUS7L antibody is un-conjugated
应用范围
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
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抗原表位
- AA 165-699
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原理
- PUS7L Antibody / Pseudouridylate synthase 7 homolog-like protein
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纯化方法
- Antigen affinity purified
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免疫原
- An E.coli-derived human recombinant protein (R165-H699) was used as the immunogen for the PUS7L antibody.
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亚型
- IgG
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anti-Pseudouridylate Synthase 7 Homolog-Like (PUS7L) (AA 1-701) antibody
PUS7L 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Pseudouridylate Synthase 7 Homolog-Like (PUS7L) (N-Term) antibodyPUS7L 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the PUS7L antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the PUS7L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- PUS7L (Pseudouridylate Synthase 7 Homolog-Like (PUS7L))
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别名
- PUS7L
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背景
- Pseudouridylate synthase 7 homolog-like protein is an enzyme that in humans is encoded by the PUS7L gene. PUS7L (pseudouridylate synthase 7 homolog (S. cerevisiae) -like) is a 701 amino acid protein that belongs to the pseudouridine synthase truD family and contains one TRUD domain. The PUS7L gene is conserved in chimpanzee, canine, bovine, mouse, chicken and zebrafish, and maps to human chromosome 12q12. 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.
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UniProt
- Q9H0K6
抗原
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