KCNJ2 (Human) Recombinant Protein (Q01)
产品名称： KCNJ2 (Human) Recombinant Protein (Q01)
英文名称： KCNJ2 (Human) Recombinant Protein (Q01)
产品编号： H00003759-Q01
产品价格： 0
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围： null
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
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- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Human KCNJ2 partial ORF ( NP_000882, 328 a.a. - 427 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- PVLFEEKHYYKVDYSRFHKTYEVPNTPLCSARDLAEKKYILSNANSFCYENEVALTSKEEDDSENGVPESTSTDTPPDIDLHNQASVPLEPRPLRRESEI
- Theoretical MW (kDa):
- 36.74
- Preparation Method:
- in vitro wheat germ expression system
- Purification:
- Glutathione Sepharose 4 Fast Flow
- Storage Buffer:
- 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
- Storage Instruction:
- Store at -80°C. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- 12.5% SDS-PAGE Stained with Coomassie Blue.
- Note:
- Best use within three months from the date of receipt of this protein.
- MSDS:
Download
- Application Image
- Enzyme-linked Immunoabsorbent Assay
- Western Blot (Recombinant protein)
- Antibody Production
- Protein Array
- Entrez GeneID:
- 3759
- GeneBank Accession#:
- NM_000891
- Protein Accession#:
- NP_000882
- Gene Name:
- KCNJ2
- Gene Alias:
- HHBIRK1,HHIRK1,IRK1,KIR2.1,LQT7,SQT3
- Gene Description:
- potassium inwardly-rectifying channel, subfamily J, member 2
- Gene Ontology:
- Hyperlink
- Gene Summary:
- Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq
- Other Designations:
- cardiac inward rectifier potassium channel,inward rectifier K+ channel KIR2.1,inward rectifier potassium channel 2,potassium inwardly-rectifying channel J2