TMIE Antikörper (AA 71-100)

Produktnummer ABIN5537885

Produktdetails anti-TMIE Antikörper

Target: TMIE (Transmembrane Inner Ear (TMIE))

Bindungsspezifität: AA 71-100

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMIE Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This TMIE antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-100 amino acids from the Central region of human TMIE.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Details zu TMIE

Target: TMIE (Transmembrane Inner Ear (TMIE))

Andere Bezeichnung: TMIE (TMIE Produkte)

Synonyme: si:ch211-163f10.1 antikoerper, DFNB6 antikoerper, 5131400L21Rik antikoerper, Mm.87012 antikoerper, sr antikoerper, RGD1562523 antikoerper, transmembrane inner ear antikoerper, tmie antikoerper, TMIE antikoerper, Tmie antikoerper

Hintergrund: This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment.

Molekulargewicht: 17 kDa

Gen-ID: 259236

UniProt: Q8NEW7

Pathways: Sensory Perception of Sound