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SOX9 anticorps (N-Term)

SOX9 Reactivité: Humain WB, IF, IHC (p), EIA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN356879
  • Antigène Voir toutes SOX9 Anticorps
    SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
    Épitope
    • 16
    • 16
    • 13
    • 10
    • 8
    • 8
    • 7
    • 6
    • 6
    • 6
    • 6
    • 6
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reactivité
    • 143
    • 69
    • 51
    • 20
    • 10
    • 6
    • 6
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Humain
    Hôte
    • 122
    • 22
    • 2
    Lapin
    Clonalité
    • 107
    • 39
    Polyclonal
    Conjugué
    • 78
    • 9
    • 8
    • 7
    • 6
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp SOX9 est non-conjugé
    Application
    • 117
    • 67
    • 44
    • 40
    • 34
    • 27
    • 27
    • 21
    • 13
    • 10
    • 7
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    Specificité
    This antibody detects SOX9 at N-term.
    Réactivité croisée (Details)
    Species reactivity (tested):Human.
    Purification
    Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS, then purified by peptide affinity purification.
    Immunogène
    This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the N-terminal region of human SOX9.
    Isotype
    Ig Fraction
    Top Product
    Discover our top product SOX9 Anticorps primaire
  • Indications d'application
    ELISA: 1/1,000. Western blot: 1/50-1/100. Immunohistochemistry. Immunofluorescence: 1/10-1/50.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.25 mg/mL
    Buffer
    PBS with 0.09 % (W/V) Sodium Azide as preservative.
    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.
    Conseil sur la manipulation
    Avoid repeated freezing and thawing.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
  • 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
    SOX9 is a member of the family of SOX (Sry-type high mobility group box) genes that were first identified on the basis of region with high homology to that of Sry (Sex determining region Y). SOX9 is a transcription factor with a high mobility group DNA-binding domain that is expressed in all prechondrocytic and chondrocytic cells during embryonic development in a pattern that close parallels that of the gene for type II collagen. SOX9 is important in neural crest formation, and is involved in regulating subsequent epithelial-mesenchymal transition and migration. 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.Synonyms: CMD1, CMPD1, SRA1, SRY (sex determining region Y)-box 9, SRY-box 9, Transcription factor SOX-9
    ID gène
    6662, 9606
    UniProt
    P48436
    Pathways
    EGFR Signaling Pathway, Stem Cell Maintenance, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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