Mouse Monoclonal DLX-3 antibody. Suitable for IHC - Wmt and reacts with Zebrafish samples.
pH: 7.5
Preservative: 0.02% Sodium azide
Constituents: 99% HEPES buffered saline
IHC - Wmt | |
---|---|
Zebrafish | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Zebrafish | Dilution info 1/100 | Notes - |
dlx3, dlx3b, Homeobox protein Dlx3b, DLX-3, Distal-less homeobox protein 3b
Mouse Monoclonal DLX-3 antibody. Suitable for IHC - Wmt and reacts with Zebrafish samples.
pH: 7.5
Preservative: 0.02% Sodium azide
Constituents: 99% HEPES buffered saline
ab174436 is produced in vitro using hybridomas grown in serum-free medium, and then concentrated by chemical fractionation. Near homogeneity as judged by SDS-PAGE.
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DLX-3 also known as Distal-less homeobox 3 is a transcription factor with a molecular weight of approximately 32 kDa. It is a member of the homeobox gene family which plays roles in developmental processes. DLX-3 is mainly expressed in tissues like skin hair follicles and the placenta. It functions by binding to specific DNA sequences causing changes in gene expression during development.
DLX-3 affects the development and differentiation processes in organisms. It interacts within a complex network of other homeobox genes influencing the development of craniofacial structures and skin. During early stages its role includes promoting cell differentiation necessary for forming specific tissues particularly in the ectoderm layer derivatives such as skin.
Several genes contribute to the pathways involving DLX-3. DLX-3 participates in the Wnt signaling and BMP pathways acting as a regulator of gene transcription necessary for cellular differentiation. It interacts with other proteins like BMP2 showing functional overlap with other members of the DLX gene family. Through these interactions DLX-3 helps coordinate proper tissue development and maintenance.
DLX-3 has associations with ectodermal dysplasias and certain craniofacial anomalies. It links to disorders like Tricho–Dento–Osseous (TDO) syndrome where mutations lead to defects in hair teeth and bone development. Apart from these DLX-3’s interactions with MSX1 highlight its role in dental and cranial disorders contributing to further understanding of hereditary conditions affecting developmental processes.
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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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ab174436 staining DLX-3 in 19 somite zebrafish by IHC-wholemount. The embryo was fixed with 4% PFA at 4°C over night and an antigen retrieval step was performed with Tris-HCl pH 9. Blocking of the sample was done with 10% sheep serum in PBS containing 01% Tween 20 and 0.5% Triton X, for 60 minutes at 23°C, followed by staining with ab174436 at 1/100 in blocking solution for 16h at 4°C. An alexa 488 conjugated goat anti-mouse polyclonal antibody at 1/1000 was used as the secondary antibody. Nuclei are stained in blue with DAPI. The forebrain is stained by Dlx3b (in green).
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