ACCN4 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2716042

Détail du produit

Antigène: ACCN4 (Amiloride-Sensitive Cation Channel 4, Pituitary (ACCN4))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette ACCN4 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human Amiloride-sensitive cation channel 4, pituitary (ACCN4), transcript variant 1 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

Antigène: ACCN4 (Amiloride-Sensitive Cation Channel 4, Pituitary (ACCN4))

Abstract: ACCN4 Produits

Synonymes: 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

Sujet: 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.

Poids moléculaire: 72 kDa

NCBI Accession: NP_061144