SOX8 Antikörper (AA 225-253)

Produktnummer ABIN5535011

Produktdetails anti-SOX8 Antikörper

Target: SOX8 (SRY (Sex Determining Region Y)-Box 8 (SOX8))

Bindungsspezifität: AA 225-253

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SOX8 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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

Immunogen: This SOX8 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 225-253 amino acids from the Central region of human SOX8.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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 SOX8

Target: SOX8 (SRY (Sex Determining Region Y)-Box 8 (SOX8))

Andere Bezeichnung: SOX8 (SOX8 Produkte)

Synonyme: SRY-box 8 antikoerper, SRY box 8 antikoerper, SRY-box 8 L homeolog antikoerper, SRY (sex determining region Y)-box 8 antikoerper, SOX8 antikoerper, Sox8 antikoerper, sox8.L antikoerper

Hintergrund: This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein may be involved in brain development and function. Haploinsufficiency for this protein may contribute to the mental retardation found in haemoglobin H-related mental retardation (ART-16 syndrome).

Molekulargewicht: 47 kDa

Gen-ID: 30812

UniProt: P57073

Pathways: Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development