Rabbit Polyclonal SOX9A antibody. N-terminal. Suitable for IHC - Wmt and reacts with Zebrafish samples. Cited in 1 publication.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 79.99% PBS, 20% Glycerol (glycerin, glycerine)
IHC - Wmt | |
---|---|
Zebrafish | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Zebrafish | Dilution info - | Notes - |
HMG box transcription factor Sox9a, Jef, Jellyfish, SRY (sex determining region Y)-box 9a, SRY box containing gene 9a, Transcription factor sox9a, wu:fj17b12, zgc:111921
Rabbit Polyclonal SOX9A antibody. N-terminal. Suitable for IHC - Wmt and reacts with Zebrafish samples. Cited in 1 publication.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 79.99% PBS, 20% Glycerol (glycerin, glycerine)
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Sox9a also known simply as Sox9 is a transcription factor with a mass of approximately 57 kDa. It acts mechanically by binding to DNA sequences to regulate the expression of various genes. This protein belongs to the SRY-related HMG-box (Sox) family which plays a part in the control of embryonic development and cell fate decisions. Sox9a is expressed in several tissues including the cartilage heart gonads and central nervous system showing its diverse role across different body parts.
Sox9a is involved in several important developmental processes. It regulates chondrogenesis the process of cartilage formation where it interacts with other proteins as part of multimeric complexes. It also plays a part in sex determination by promoting the development of Sertoli cells in testes affecting male gonad differentiation. Sox9a's function in the regulation of stem cells signifies its regulatory potential in tissue renewal and repair mechanisms.
Sox9a plays a role in both the TGF-beta and Wnt signaling pathways essential for the differentiation and proliferation of cells. In the TGF-beta pathway Sox9a works closely with Smad3 to influence the transcription of genes necessary for chondrocyte differentiation. In the context of the Wnt signaling pathway Sox9a interacts with β-catenin being part of a regulatory network that affects skeletal development and repair.
Abnormalities in Sox9a function or expression relate to campomelic dysplasia a disorder characterized by skeletal malformations and sex reversal. Mutations in Sox9a lead to defective cartilage development and improper sexual differentiation. Another related condition is Pierre Robin sequence often featuring craniofacial anomalies which involve disruptions in skeletal and craniofacial development pathways where Sox9a and the protein RUNX2 have roles in bone formation.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Immunohistochemical analysis (whole mount) of paraformaldehyde-fixed Zebrafish embryo labeling Sox9a with ab209820 at 1/200 dilution.
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