SOX3 anticorps

N° du produit ABIN6654139

Détail du produit anti-SOX3 anticorps

Antigène: SOX3 (SRY (Sex Determining Region Y)-Box 3 (SOX3))

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SOX3 est non-conjugé

Application: Western Blotting (WB)

Purification: Antigen affinity purified

Immunogène: Amino acids DAADAASPLPGGRLHGVHQHYQGAGTAVNGTVPLTHI were used as the immunogen for the SOX3 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the SOX3 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL

Restrictions: For Research Use only

Stockage

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: -20 °C

Stockage commentaire: After reconstitution, the SOX3 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur SOX3

Antigène: SOX3 (SRY (Sex Determining Region Y)-Box 3 (SOX3))

Autre désignation: SOX3 (SOX3 Produits)

Synonymes: anticorps GHDX, anticorps MRGH, anticorps PHP, anticorps PHPX, anticorps SOXB, anticorps CH3, anticorps Sry, anticorps Xlsox3, anticorps Xtsox3, anticorps mrgh, anticorps soxb, anticorps xSox3, anticorps Sox-3, anticorps fc93f07, anticorps id:ibd2036, anticorps sb:cb493, anticorps wu:fc93f07, anticorps wu:fd02a08, anticorps zgc:110279, anticorps sox3-a, anticorps xSox-B1, anticorps SRY-box 3, anticorps transcription factor SOX-3, anticorps SRY (sex determining region Y)-box 3, anticorps SRY-box 3 S homeolog, anticorps SOX3, anticorps Tsp_06143, anticorps sox3, anticorps Sox3, anticorps sox3.S

Sujet: Transcription factor SOX-3 is a protein that in humans is encoded by the SOX3 gene. 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. Mutations in this gene have been associated with X-linked cognitive disability with growth hormone deficiency.

UniProt: P41225