- ￥1425 - 3930
- Leading Biology
- APR30266N
- 美国
- 2025年07月10日
- IHC (Mus musculus)
- Rabbit
- Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 靶点：
G6pt; G6Pase; AW107337; Glc-6-Pase
- 浓度：
Affinity purification
- 应用范围：
IHC (Mus musculus)
- 宿主：
Rabbit
- 适应物种：
Mouse
- 保质期：
1-2年
- 供应商：
安诺伦（北京）生物科技有限公司
- 保存条件：
Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
- 形态：
形式：Liquid 储存溶液：Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
- 亚型：
IgG
- 免疫原：
A synthetic peptide of Mouse G6PC.
- 规格：
50 µl/100 µl/200 µl
| 规格： | 50 µl | 产品价格： | ￥1425.0 |
|---|---|---|---|
| 规格： | 100 µl | 产品价格： | ￥2370.0 |
| 规格： | 200 µl | 产品价格： | ￥3930.0 |
Observed MW: 40KDa
稀释方法：WB 1:1000 - 1:2000
IF 1:50 - 1:200
总结：The enzyme encoded by this gene is a multisubunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for glucose-6-phosphate, inorganic phosphate, and glucose. This gene is one of three glucose-6-phosphatase catalytic-subunit-encoding genes in mouse. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1).
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文献和实验= NAL), appears to form upon oxidative cyclization of the nonfluorescent 2:1 lysine-HNE Michael adduct-Schiff base cross-link (Scheme 1). Polyclonal antibody (PAb) to the NAL-HNE fluorophore was raised in rabbit and found to be highly specific
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