AMPD1 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-16156
宿主: Rabbit
反应性: H
应用: WB,IHC
Overview
| Synonyms | Adenosine monophosphate deaminase 1 (isoform M),Adenosine monophosphate deaminase 1,AMP deaminase 1,AMP deaminase isoform M,AMPD 1,AMPD,Ampd01,MAD,MADA,Myoadenylate deaminase,RATAMPD01,Skeletal muscle AMPD,AMPD1抗体 |
| Swissprot | P23109 |
| Source | Rabbit |
| Reactivity | Human |
| Immunogen | Synthetic peptide of human AMPD1 |
| Application | WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213) |
| Recommended dilution | WB,,1:500-1:2000;IHC,,1:100-1:300; |
| Concentration | 0.5 mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Cytosol |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
| Background | Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. |
Images
Western Blot analysis of Human fetal muscle tissue using AMPD1 Polyclonal Antibody at dilution of 1:1600
Immunohistochemistry of paraffin-embedded Human liver cancer using AMPD1 Polyclonal Antibody at dilution of 1:70
Immunohistochemistry of paraffin-embedded Human thyroid cancer using AMPD1 Polyclonal Antibody at dilution of 1:70
