SOX9 polyclonal antibody
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More Files
- More Functions
Western Blot (Cell lysate)
Western blot analysis of SOX9 polyclonal antibody (Cat # PAB2489) in HepG2 cell line lysates (35 ug/lane). SOX9 (arrow) was detected using the purified polyclonal antibody.
Flow Cytometry
Flow cytometric analysis of HepG2 cells using SOX9 polyclonal antibody (Cat # PAB2489)(bottom histogram) compared to a negative control cell (top histogram).
FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
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Specifications
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of SOX9.
Immunogen
A synthetic peptide (conjugated with KLH) corresponding to internal region of human SOX9.
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Ammonium sulfate precipitation
Recommend Usage
Western Blot (1:1000)
Flow cytometry (1:10-50)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western blot analysis of SOX9 polyclonal antibody (Cat # PAB2489) in HepG2 cell line lysates (35 ug/lane). SOX9 (arrow) was detected using the purified polyclonal antibody.Flow Cytometry
Flow cytometric analysis of HepG2 cells using SOX9 polyclonal antibody (Cat # PAB2489)(bottom histogram) compared to a negative control cell (top histogram).
FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis. -
Gene Info — SOX9
Entrez GeneID
6662Protein Accession#
NP_000337;P48436Gene Name
SOX9
Gene Alias
CMD1, CMPD1, SRA1
Gene Description
SRY (sex determining region Y)-box 9
Gene Ontology
HyperlinkGene Summary
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
Other Designations
SRY (sex determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal)|SRY (sex-determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal)|SRY (sex-determining region Y)-box 9 protein|campomelic dysplasia, autosomal sex-revers
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Interactomes
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Diseases
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Publication Reference
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SOX9 is a key player in ultraviolet B-induced melanocyte differentiation and pigmentation.
Passeron T, Valencia JC, Bertolotto C, Hoashi T, Le Pape E, Takahashi K, Ballotti R, Hearing VJ.
PNAS 2007 Aug; 104(35):13984.
Application：ICC, IF, IHC, IP, WB, Human, a-LP NHM cells, Human skin.
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Expression and biological role of the prostaglandin D synthase/SOX9 pathway in human ovarian cancer cells.
Malki S, Bibeau F, Notarnicola C, Roques S, Berta P, Poulat F, Boizet-Bonhoure B.
Cancer Letters 2007 Oct; 255(2):182.
Application：IF, IHC-P, WB-Tr, Human, BG1, Cov434 cells, Ovarian tumors.
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SOX9 is a key player in ultraviolet B-induced melanocyte differentiation and pigmentation.
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