SOX9 anticorps
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- Antigène Voir toutes SOX9 Anticorps
- SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp SOX9 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
- Fonction
- SOX9 Rabbit mAb
- Réactivité croisée
- Humain, Souris, Rat
- Attributs du produit
- Monoclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- A synthesized peptide derived from human SOX9.
- Isotype
- IgG
- Top Product
- Discover our top product SOX9 Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200,IP,1:50 - 1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
- 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.
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- Antigène
- SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
- Autre désignation
- SOX9 (SOX9 Produits)
- Synonymes
- anticorps CMD1, anticorps CMPD1, anticorps SRA1, anticorps LOC100227849, anticorps 2010306G03Rik, anticorps AV220920, anticorps mKIAA4243, anticorps SOX-9, anticorps cmd1, anticorps cmpd1, anticorps sox-9, anticorps sox9, anticorps sox9-a, anticorps sox9-b, anticorps sox9b, anticorps sra1, anticorps SRY-box 9, anticorps transcription factor SOX-9, anticorps SRY (sex determining region Y)-box 9, anticorps SRY box 9, anticorps SRY-box 9 L homeolog, anticorps SOX9, anticorps LOC100227849, anticorps Sox9, anticorps sox9.L
- 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. [provided by RefSeq, Jul 2008],CMD1,CMPD1,SRA1,SRXX2,SRXY10,SOX9,SRY-box 9,Apoptosis,Cell Biology & Developmental Biology,Epigenetics & Nuclear Signaling,Mesenchymal Stem Cells,Neural Stem Cells,Neuroscience,Stem Cells,Transcription Factors,SOX9
- Poids moléculaire
- 70kDa
- ID gène
- 6662
- UniProt
- P48436
- Pathways
- EGFR Signaling Pathway, Stem Cell Maintenance, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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