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Anti-ATP13A2 Polyclonal Antibody
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Catalog No. TMAB-02939
Anti-ATP13A2 Polyclonal Antibody is a Rabbit antibody targeting ATP13A2. Anti-ATP13A2 Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
Anti-ATP13A2 Polyclonal Antibody
Anti-ATP13A2 Polyclonal Antibody
😃Good
Catalog No. TMAB-02939
Anti-ATP13A2 Polyclonal Antibody is a Rabbit antibody targeting ATP13A2. Anti-ATP13A2 Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 50 μL | $220 | 7-10 days | 7-10 days | |
| 100 μL | $372 | 7-10 days | 7-10 days | |
| 200 μL | $529 | 7-10 days | 7-10 days |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Antigen Details
Chemical Properties
| Description | Anti-ATP13A2 Polyclonal Antibody is a Rabbit antibody targeting ATP13A2. Anti-ATP13A2 Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF. |
| Ig Type | IgG |
| Reactivity | Rat (predicted:Human,Mouse,Pig,Cow,Horse,Rabbit) |
| Application | |
| Recommended Dose | IHC-P: 1:100-500; IHC-Fr: 1:100-500; IF: 1:100-500 |
| Antibody Type | Polyclonal |
| Host Species | Rabbit |
| Subcellular Localization | Membrane; Multi-pass membrane protein (By similarity). Lysosome. |
| Tissue Specificity | Expressed in brain; protein levels are markedly increased in brain from subjects with Parkinson disease and subjects with dementia with Lewy bodies. Detected in pyramidal neurons located throughout the cingulate cortex (at protein level). In the substantia nigra, it is found in neuromelanin-positive dopaminergic neurons (at protein level). |
| Construction | Polyclonal Antibody |
| Purification | Protein A purified |
| Appearance | Liquid |
| Formulation | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Concentration | 1mg/ml |
| Research Background | ATP13A2 is a 1,180 amino acid multi-pass membrane protein that belongs to the P5 subfamily of ATPases which play an important role in the transportation of inorganic cations. Expressed as multiple alternative spliced isoforms, ATP13A2 functions to catalyze the conversion of ATP to ADP and a free phosphate, thereby participating in the active transport of ions across cellular membranes. Defects in the gene encoding ATP13A2 are the cause of Kufor-Rakeb syndrome (KRS), a rare hereditary type of Parkinson’s disease that exhibits juvenile onset and is characterized by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. |
| Immunogen | KLH conjugated synthetic peptide: human ATP13A2 |
| Antigen Species | Human |
| Gene Name | ATP13A2 |
| Gene ID | |
| Protein Name | Polyamine-transporting ATPase 13A2 |
| Uniprot ID | |
| Function | May play a role in intracellular cation homeostasis and the maintenance of neuronal integrity. |
| Molecular Weight | Theoretical: 129 kDa. |
Stability & Storage
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
| Transport | Shipping with blue ice. |
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