ARG45604
anti-AMPD1 antibody
anti-AMPD1 antibody for Flow cytometry,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat
Overview
| Product Description | Rabbit Polyclonal antibody recognizes AMPD1 |
|---|---|
| Tested Reactivity | Hu, Ms, Rat |
| Tested Application | FACS, IHC-P, WB |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Target Name | AMPD1 |
| Antigen Species | Human |
| Immunogen | Recombinant protein containing to human AMPD1. |
| Conjugation | Un-conjugated |
| Alternate Names | AMPD1; Adenosine Monophosphate Deaminase 1; Myoadenylate Deaminase; MADA; MAD; Adenosine Monophosphate Deaminase 1 (Isoform M); Skeletal Muscle AMPD; AMP Deaminase 1; EC 3.5.4.6; Adenosine Monophosphate Deaminase-1 (Muscle); AMP Deaminase Isoform M; AMPD Isoform M; MMDD; AMPD |
Application Instructions
| Application Suggestion |
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| Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Form | Liquid |
|---|---|
| Purification | Affinity purified |
| Buffer | 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose. |
| Stabilizer | 4% Trehalose |
| Concentration | 0.5 mg/ml |
| Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
| Database Links | |
|---|---|
| Gene Symbol | AMPD1 |
| Gene Full Name | Adenosine Monophosphate Deaminase 1 |
| 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.[provided by RefSeq, Feb 2010] |
| Function | AMP deaminase plays a critical role in energy metabolism. [UniProt] |
| Cellular Localization | Cytosol. [UniProt] |
| Calculated MW | 63 kDa |
| PTM | Phosphoprotein. [UniProt] |
Images (5) Click the Picture to Zoom In
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ARG45604 anti-AMPD1 antibody IHC-P image
Immunohistochemistry: Human breast cancer stained with ARG45604 anti-AMPD1 antibody at 2 μg/ml dilution.
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ARG45604 anti-AMPD1 antibody WB image
Western blot: MCF-7 stained with ARG45604 anti-AMPD1 antibody at 0.5 μg/ml dilution.
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ARG45604 anti-AMPD1 antibody FACS image
Flow Cytometry: U251 stained with ARG45604 anti-AMPD1 antibody at 1 µg/10^6 cells dilution.
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ARG45604 anti-AMPD1 antibody WB image
Western blot: Rat heart stained with ARG45604 anti-AMPD1 antibody at 0.5 μg/ml dilution.
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ARG45604 anti-AMPD1 antibody WB image
Western blot: Mouse skeletal muscle stained with ARG45604 anti-AMPD1 antibody at 0.5 μg/ml dilution.
