抗体

IRK13 rabbit Polyclonal Antibody

IRK13抗体
IRK13抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily J member 13(KCNJ13) Homo sapiens This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010],

IRK14 rabbit Polyclonal Antibody

IRK14抗体
IRK14抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily J member 14(KCNJ14) Homo sapiens 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, and probably has a role in controlling the excitability of motor neurons. [provided by RefSeq, Feb 2013],

IRK15 rabbit Polyclonal Antibody

IRK15抗体
IRK15抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily J member 15(KCNJ15) Homo sapiens 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 has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Eight transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2013],

IRK6 rabbit Polyclonal Antibody

IRK6抗体
IRK6抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily J member 6(KCNJ6) Homo sapiens This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015],

IRK8 rabbit Polyclonal Antibody

IRK8抗体
IRK8抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily J member 8(KCNJ8) Homo sapiens 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, is controlled by G-proteins. Defects in this gene may be a cause of J-wave syndromes and sudden infant death syndrome (SIDS). [provided by RefSeq, May 2012],

IRPL1 rabbit Polyclonal Antibody

IRPL1抗体
IRPL1抗体应用:WB 1:500-2000 ELISA 1:5000-20000interleukin 1 receptor accessory protein like 1(IL1RAPL1) Homo sapiens The protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. It is most closely related to interleukin 1 receptor accessory protein-like 2 (IL1RAPL2). This gene and IL1RAPL2 are located at a region on chromosome X that is associated with X-linked non-syndromic mental retardation. Deletions and mutations in this gene were found in patients with mental retardation. This gene is expressed at a high level in post-natal brain structures involved in the hippocampal memory system, which suggests a specialized role in the physiological processes underlying memory and learning abilities. [provided by RefSeq, Jul 2008],

ISG15 rabbit Polyclonal Antibody

ISG15抗体
ISG15抗体应用:WB 1:500-2000 ELISA 1:5000-20000ISG15 ubiquitin-like modifier(ISG15) Homo sapiens The protein encoded by this gene is a ubiquitin-like protein that is conjugated to intracellular target proteins upon activation by interferon-alpha and interferon-beta. Several functions have been ascribed to the encoded protein, including chemotactic activity towards neutrophils, direction of ligated target proteins to intermediate filaments, cell-to-cell signaling, and antiviral activity during viral infections. While conjugates of this protein have been found to be noncovalently attached to intermediate filaments, this protein is sometimes secreted. [provided by RefSeq, Dec 2012],

ISG20 rabbit Polyclonal Antibody

ISG20抗体
ISG20抗体应用:WB 1:500-2000

ISK4 rabbit Polyclonal Antibody

ISK4抗体
ISK4抗体应用:IHC-p 1:50-200

ISLR2 rabbit Polyclonal Antibody

ISLR2抗体
ISLR2抗体应用:WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 1 Ig-like (immunoglobulin-like) domain.,similarity:Contains 5 LRR (leucine-rich) repeats.,
沪ICP备15039594号-4
在线客服
专业的客服团队,欢迎在线资讯
客服时间: 周一至周五9:00 - 18:00