SOX9 anticorps (AA 351-450)

N° du produit ABIN6945007

L’anticorps anti-SOX9 Polyclonal Lapin est utilisé pour la détection de SOX9 dans des échantillons de Humain. Il a été validé pour WB, FACS, IHC (p), IF (p), IF (cc) et IHC (fro).

Aperçu rapide pour SOX9 anticorps (AA 351-450) (ABIN6945007)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SOX9 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-SOX9 anticorps

Épitope: AA 351-450

Fonction: SOX9 Polyclonal Antibody

Réactivité croisée: Humain, Souris, Rat

Homologie: Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SOX9

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000),

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

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: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur SOX9

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

Autre désignation: SOX9

Sujet:

Synonyms: CMD 1, CMD1, CMPD 1, CMPD1, SOX 9, Sox9, SOX9_HUMAN, SRA 1, SRA1 antibody 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, Transcription factor SOX 9, Transcription factor SOX-9, transcription factor SOX9, campomelic dysplasia autosomal sex reversal.

Background: 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. [provided by RefSeq].

ID gène: 6662

UniProt: P48436

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