SRY (Sex Determining Region Y)-Box 9 (SOX9) Peptide
SOX9
Reactivité: Humain
Hôte: Synthetic
BP, WB, FACS
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- Antigène Tous les produits SOX9
- SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Flow Cytometry (FACS)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-SOX9 antibody (Catalog #: ARP37986_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
- Synonymes
- CMD1 Peptide, CMPD1 Peptide, SRA1 Peptide, LOC100227849 Peptide, 2010306G03Rik Peptide, AV220920 Peptide, mKIAA4243 Peptide, SOX-9 Peptide, cmd1 Peptide, cmpd1 Peptide, sox-9 Peptide, sox9 Peptide, sox9-a Peptide, sox9-b Peptide, sox9b Peptide, sra1 Peptide, SRY-box 9 Peptide, transcription factor SOX-9 Peptide, SRY (sex determining region Y)-box 9 Peptide, SRY box 9 Peptide, SRY-box 9 L homeolog Peptide, SOX9 Peptide, LOC100227849 Peptide, Sox9 Peptide, sox9.L Peptide
- Sujet
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SOX9 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.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: CMD1, CMPD1, SRA1
Protein Interaction Partner: KPNB1,CREB1,CREBBP,EP300,HSPA1A,KPNB1,MAF,MED12,NR5A1,SPEN,TRAF2,HSPA1A,MAF,MED12,NR5A1
Protein Size: 509 - Poids moléculaire
- 56 kDa
- ID gène
- 6662
- NCBI Accession
- NM_000346, NP_000337
- UniProt
- P48436
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