POU4F3 Antikörper (AA 1-180)

Produktnummer ABIN6145985

Produktdetails anti-POU4F3 Antikörper

Target: POU4F3 (POU Domain, Class 4, Transcription Factor 3 (POU4F3))

Bindungsspezifität: AA 1-180

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser POU4F3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MMAMNSKQPF GMHPVLQEPK FSSLHSGSEA MRRVCLPAPQ LQGNIFGSFD ESLLARAEAL AAVDIVSHGK NHPFKPDATY HTMSSVPCTS TSSTVPISHP AALTSHPHHA VHQGLEGDLL EHISPTLSVS GLGAPEHSVM PAQIHPHHLG AMGHLHQAMG MSHPHTVAPH SAMPACLSDV

Kreuzreaktivität: Human

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human POU4F3 (NP_002691.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu POU4F3

Target: POU4F3 (POU Domain, Class 4, Transcription Factor 3 (POU4F3))

Andere Bezeichnung: POU4F3 (POU4F3 Produkte)

Synonyme: POU4F3 antikoerper, BRN-3 antikoerper, BRN3 antikoerper, BRN3C antikoerper, DFNA15 antikoerper, BRN-3.1 antikoerper, brn-3c antikoerper, brn3.1 antikoerper, brn3c antikoerper, Brn3.1 antikoerper, Brn3c antikoerper, ddl antikoerper, dreidel antikoerper, POU class 4 homeobox 3 antikoerper, POU domain, class 4, transcription factor 3 antikoerper, POU4F3 antikoerper, Pou4f3 antikoerper, pou4f3 antikoerper

Hintergrund: This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.,POU4F3,BRN3C,DFNA15,DFNA42,DFNA52,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Apoptosis,Neuroscience,POU4F3

Molekulargewicht: 37 kDa

Gen-ID: 5459

UniProt: Q15319

Pathways: Sensory Perception of Sound