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PANP/C12orf53 Protein, Human, Recombinant (hFc)

PANP/C12orf53 Protein, Human, Recombinant (hFc)

产品编号 TMPY-02961
别名: C12orf53, UNQ828/PRO1755, PILR α associated neural protein, PANP, leda-1, PILR alpha associated neural protein, LEDA1

C12orf53 is mainly expressed in adult brain and cerebellum. It also can be detected in fetal brain and virtually no expression in spleen, heart, kidney, liver and dorsal ganglion relative to brain. C12orf53 acts as a ligand for PILRA in neural tissues, where it may be involved in immune regulation. Chromosome 12 encodes over 1,100 genes within 132 million bases. 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 class I interaction.

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PANP/C12orf53 Protein, Human, Recombinant (hFc)
规格 价格/CNY 货期 数量
100 μg ¥ 4,460 5日内发货
618惊喜特惠 4重福利大放送
药物设计专题培训
千万补贴 助力科研
产品目录号及名称: PANP/C12orf53 Protein, Human, Recombinant (hFc) (TMPY-02961)
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生物活性 Testing in progress
产品描述 C12orf53 is mainly expressed in adult brain and cerebellum. It also can be detected in fetal brain and virtually no expression in spleen, heart, kidney, liver and dorsal ganglion relative to brain. C12orf53 acts as a ligand for PILRA in neural tissues, where it may be involved in immune regulation. Chromosome 12 encodes over 1,100 genes within 132 million bases. 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 class I interaction.
种属 Human
表达系统 HEK293 Cells
标签 C-hFc
蛋白编号 Q8IYJ0-1
别名 C12orf53, UNQ828/PRO1755, PILR α associated neural protein, PANP, leda-1, PILR alpha associated neural protein, LEDA1
蛋白构建 The Human C12orf53 (Q8IYJ0-1) (Met1-Pro178) was expressed, fused with the Fc region of Human IgG1 at the C-terminus.
蛋白纯度 > 96 % as determined by SDS-PAGE
分子量 42.3 kDa (predicted)
内毒素 < 1.0 EU/μg of the protein as determined by the LAL method.
缓冲液 Lyophilized from a solution filtered through a 0.22 μm filter, containing PBS, pH 7.4. Typically, a mixture containing 5% to 8% trehalose, mannitol, and 0.01% Tween 80 is incorporated as a protective agent before lyophilization.
复溶方法 A Certificate of Analysis (CoA) containing reconstitution instructions is included with the products. Please refer to the CoA for detailed information.
存储

It is recommended to store recombinant proteins at -20°C to -80°C for future use. Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.

运输方式

In general, Lyophilized powders are shipping with blue ice.

研究背景 C12orf53 is mainly expressed in adult brain and cerebellum. It also can be detected in fetal brain and virtually no expression in spleen, heart, kidney, liver and dorsal ganglion relative to brain. C12orf53 acts as a ligand for PILRA in neural tissues, where it may be involved in immune regulation. Chromosome 12 encodes over 1,100 genes within 132 million bases. 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 class I interaction.

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Keywords

PANP/C12orf53 Protein, Human, Recombinant (hFc) C12orf53 UNQ828/PRO1755 PILR α associated neural protein PANP leda-1 UNQ828/PRO 1755 LEDA 1 UNQ828/PRO-1755 PILR a associated neural protein LEDA-1 PILR alpha associated neural protein LEDA1 recombinant recombinant-proteins proteins protein

 

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