SOX9 anticorps (Ser181)

N° du produit ABIN5960080

Cet anticorps anti-SOX9 est un anticorps Lapin Polyclonal détectant SOX9 dans WB, ELISA, IF et IHC (p). Adapté pour Humain et Souris.

Aperçu rapide pour SOX9 anticorps (Ser181) (ABIN5960080)

Antigène: SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SOX9 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-SOX9 anticorps

Épitope: Ser181

Specificité: Campomelic dysplasia autosomal sex reversal,CMD 1,CMD1,CMPD 1,CMPD1,SOX 9,Sox9,SOX9,SRA 1,SRA1,SRXX2,SRXY10,SRY (sex determining region Y) box 9 (campomelic dysplasia autosomal,SRY (sex determining region Y) box 9,SRY (sex determining region Y)-box 9,SRY (sex-determining region Y)-box 9 protein,SRY related HMG box gene 9,Transcription factor SOX 9,Transcription factor SOX-9,transcription factor SOX9

Purification: Affinity purification

Immunogène: Synthesized peptide derived from human Sox-9 around the non-phosphorylation site of Ser181.

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:100-1:300, IF 1:200-1:1000, ELISA 1:5000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 0.5 % BSA and 50 % glycerol,  pH 7.4

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur SOX9

Antigène: SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))

Autre désignation: Sox-9

Sujet: The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal.

Poids moléculaire: 56kDa

ID gène: 6662

UniProt: P48436

Pathways: EGFR Signaling Pathway, Stem Cell Maintenance, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development