KCNJ2 (Human) Recombinant Protein (Q01)
產品名稱： KCNJ2 (Human) Recombinant Protein (Q01)
英文名稱： KCNJ2 (Human) Recombinant Protein (Q01)
產品編號： H00003759-Q01
產品價格： 0
產品產地： 臺灣
品牌商標： Abnova
更新時間： null
使用范圍： null
亞諾法生技股份有限公司（Abnova)
- 聯系人 :
- 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區域 : 臺灣
- 電話 : +886-920**1152 點擊查看
- 傳真 : 點擊查看
- 郵箱 : 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