AMPD1 抗体 (AA 500-550)
Quick Overview for AMPD1 抗体 (AA 500-550) (ABIN372278)
抗原
See all AMPD1 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 500-550
-
特异性
- This antibody recognizes AMPD1.
-
交叉反应 （详细）
-
Species reactivity (expected):Bovine, Chimpanzee, Monkey, Mouse, Rat and Zebrafish.
Species reactivity (tested):Human. -
纯化方法
- Immunoaffinity Chromatography.
-
免疫原
- Synthetic peptide corresponding to a portion of the amino acids 500-550 of Human AMPD1.
-
亚型
- IgG
-
-
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) (AA 50-260) antibody
AMPD1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) antibodyAMPD1 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) (AA 101-200) antibodyAMPD1 适用: 小鼠, 大鼠 ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) (AA 97-272) antibodyAMPD1 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
-
Immunohistochemistry on Paraffin Sections: 5-10 μg/mL. Western Blot: 0.5-2.0 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. -
限制
- 仅限研究用
-
-
-
浓度
- 0.5 mg/mL
-
缓冲液
- PBS containing 0.05 % Sodium Azide as preservative and 0.2 % Gelatin as stabilizer.
-
储存液
- Sodium azide
-
注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
注意事项
- Avoid repeated freezing and thawing.
-
储存条件
- 4 °C/-20 °C
-
储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
-
-
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
-
别名
- AMP Deaminase 1 / AMPD1
-
背景
- AMP deaminase (AMPD) is an allosteric enzyme that plays a critical role in energy metabolism. There are three functional isoforms of AMPD. AMPD1 is the skeletal muscle-specific isoform M located in type II muscle fibers, neuromuscular junctions and in capillaries. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type (AMPDDM). AMPDDM is a metabolic disorder resulting in exercise-related myopathy. It is characterized by exercise-induced muscle aches, cramps, and early fatigue.Synonyms: AMP deaminase isoform M, Myoadenylate deaminase
-
分子量
- 87 kDa.
-
基因ID
- 270
-
NCBI登录号
- NP_000027
-
UniProt
- P23109
抗原
-
