- ￥6600
- GeneTex
- 美国
- GTX23625
- 2025年07月16日
- WB, IP, ChIP assay
- Rabbit
- Human, Mouse, Rat, Rabbit, Pig
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
The immunogen recognized by this antibody maps to a region between residue 475 and 525 of human ATPase, Ca++ transporter, cardiac muscle, slow twitch 2 using the numbering given in entry NP_733765.1 (GeneID 488).
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. Store at 4ºC. DO NOT FREEZE.
- 克隆性：
Polyclonal
- 标记物：
Unconjugated
- 适应物种：
Human, Mouse, Rat, Rabbit, Pig
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX23625
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, IP, ChIP assay
- 浓度：
1 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
SERCA2 ATPase
- 抗体英文名：
SERCA2 ATPase antibody
- 抗体名：
SERCA2 ATPase 抗体
- 规格：
50 μl
IP analysis of 293T cell lysate using GTX23625 SERCA2 ATPase antibody.
IP protein : 0.5 -1.0 mg
Dilution : 1 μg/ml for WB ; 0.5-1 mg lysate / 6μg antibody for IP reaction
Loading: 20% of IP loaded
WB analysis of HeLa, 293T, Jurkat, TCMK-1, and NIH3T3 cell lysates (in NETN lysis buffer) using GTX23625 SERCA2 ATPase antibody.
Loading : 50μg
Dilution : 1 μg/ml
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文献和实验Cantero-Recasens G et al., Hum Mol Genet 2010 (PMID:19819884)
Ca2+ signaling plays an essential role in several functions of cardiac myocytes. Transient rises and reductions of cytosolic Ca2+ , permitted by the sarcoplasmic reticulum Ca2+ ATPase (SERCA2) and other proteins, control each cycle
Transgenic Mouse Models for Cardiac Dysfunction by a Specific Gene Manipulation
The sarcoplasmic reticulum Casn+2 ATPase (SERCA) plays a pivotal role in calcium cycling and the beat-to-beat function of the heart. Recent studies have shown that decreased expression and activity of SERCA are associated with end-stage heart
where the protein is located. In this example, we will use antibodies for the calcium ATPase, or pump, that is located in the endoplasmic reticulum (ER) of very cell. The antibody used here only recognized the chicken calcium ATPase but immunofluorescence
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