SOX18 anticorps

N° du produit ABIN7469025

Cet anticorps Lapin Polyclonal détecte spécifiquement SOX18 dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour SOX18 anticorps (ABIN7469025)

Antigène: SOX18 (SRY (Sex Determining Region Y)-Box 18 (SOX18))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SOX18 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SOX18 anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human SOX18. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:5000-1:20000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: human SOX18-transfected 293T cells

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur SOX18

Antigène: SOX18 (SRY (Sex Determining Region Y)-Box 18 (SOX18))

Autre désignation: SRY-box 18

Sujet:

Synonyms: SRY-box 18 , HLTRS , HLTS

Background: 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 regulator after forming a protein complex with other proteins. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. [provided by RefSeq]

Poids moléculaire: 41 kDa

ID gène: 54345

UniProt: P35713