KCNE3 polyclonal antibody
产品名称: KCNE3 polyclonal antibody
英文名称: KCNE3 polyclonal antibody
产品编号: PAB18745
产品价格: null
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围:
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
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Goat polyclonal antibody raised against synthetic peptide of KCNE3.
- Immunogen:
- A synthetic peptide corresponding to amino acids at internal region of human KCNE3.
- Sequence:
- C-PDNQTEERRASLP
- Host:
- Goat
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (1:1000)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Application Image
- ELISA
- Entrez GeneID:
- 10008
- Protein Accession#:
- NP_005463.1
- Gene Name:
- KCNE3
- Gene Alias:
- DKFZp781H21101,HOKPP,MGC102685,MGC129924,MiRP2
- Gene Description:
- potassium voltage-gated channel, Isk-related family, member 3
- Gene Ontology:
- Hyperlink
- Gene Summary:
- Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, isk-related subfamily. This member is a type I membrane protein, and a beta subunit that assembles with a potassium channel alpha-subunit to modulate the gating kinetics and enhance stability of the multimeric complex. This gene is prominently expressed in the kidney. A missense mutation in this gene is associated with hypokalemic periodic paralysis. [provided by RefSeq
- Other Designations:
- cardiac voltage-gated potassium channel accessory subunit,minK-related peptide 2,minimum potassium ion channel-related peptide 2,potassium voltage-gated channel subfamily E member 3,voltage-gated K+ channel subunit MIRP2