ACCN4 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Target See all ACCN4 Proteins
- ACCN4 (Amiloride-Sensitive Cation Channel 4, Pituitary (ACCN4))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 2
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This ACCN4 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human ASIC4 / ACCN4 (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product ACCN4 Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- ACCN4 (Amiloride-Sensitive Cation Channel 4, Pituitary (ACCN4))
- Alternative Name
- Asic4,accn4 (ACCN4 Products)
- Synonyms
- ACCN4 Protein, BNAC4 Protein, Accn4 Protein, Spasic Protein, acid sensing ion channel subunit family member 4 S homeolog Protein, acid sensing ion channel subunit family member 4 Protein, acid-sensing (proton-gated) ion channel family member 4 Protein, asic4.S Protein, ASIC4 Protein, Asic4 Protein
- Background
- This gene belongs to the superfamily of acid-sensing ion channels, which are proton-gated, amiloride-sensitive sodium channels. These channels have been implicated in synaptic transmission, pain perception as well as mechanoperception. This gene is predominantly expressed in the pituitary gland, and was considered a candidate for paroxysmal dystonic choreoathetosis (PDC), a movement disorder, however, no correlation was found between mutations in this gene and PDC.
- Molecular Weight
- 69.9 kDa
- NCBI Accession
- NP_878267
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