BSND Antikörper (Middle Region)

Produktnummer ABIN567558

Der Kaninchen Polyklonal anti-BSND Antikörper (ABIN567558) detektiert spezifisch BSND in WB. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für BSND Antikörper (Middle Region) (ABIN567558)

Target: BSND (Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BSND Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-BSND Antikörper

Bindungsspezifität: Middle Region

Sequenz: PNASPHDREE ACSPQQEPQG CRCPLDRFQD FALIDAPTLE DEPQEGQQWE

Homologie: Human: 100%

Produktmerkmale: This is a rabbit polyclonal antibody against BSND. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of human BSND

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 320 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu BSND

Target: BSND (Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND))

Andere Bezeichnung: BSND

Hintergrund: This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness.
Alias Symbols: BART, DFNB73, MGC119283, MGC119284, MGC119285
Protein Interaction Partner: FATE1, APP,
Protein Size: 320

Molekulargewicht: 35 kDa

Gen-ID: 7809

NCBI Accession: NM_057176, NP_476517

UniProt: Q8WZ55

Pathways: Sensory Perception of Sound