SCNN1A anticorps (AA 182-429)

N° du produit ABIN1886132

Détail du produit anti-SCNN1A anticorps

Antigène: SCNN1A (Sodium Channel, Nonvoltage-Gated 1 alpha (SCNN1A))

Épitope: AA 182-429

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SCNN1A est non-conjugé

Application: Western Blotting (WB)

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 182 and 429 of SCNN1A

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur SCNN1A

Antigène: SCNN1A (Sodium Channel, Nonvoltage-Gated 1 alpha (SCNN1A))

Autre désignation: SCNN1A (SCNN1A Produits)

Synonymes: anticorps BESC2, anticorps ENaCa, anticorps ENaCalpha, anticorps SCNEA, anticorps SCNN1, anticorps ENaC, anticorps Scnn1, anticorps mENaC, anticorps SCNN1A, anticorps alphaxENaC, anticorps besc2, anticorps enaca, anticorps scnn1, anticorps ENAC, anticorps sodium channel epithelial 1 alpha subunit, anticorps sodium channel, nonvoltage-gated 1 alpha, anticorps sodium channel, non voltage gated 1 alpha subunit L homeolog, anticorps Scnn1a, anticorps SCNN1A, anticorps scnn1a.L

Sujet: Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs.These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma.This gene encodes the alpha subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), a rare salt wasting disease resulting from target organ unresponsiveness to mineralocorticoids.Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq]

Poids moléculaire: 76 kDa

ID gène: 6337

NCBI Accession: NM_001038, NP_001029