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The antibody against SOX14 was raised in rabbit using the Recombinant Human Transcription factor SOX-14 protein (1-137AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC, IF.
The antibody against SOX14 was raised in rabbit using the Recombinant Human Transcription factor SOX-14 protein (1-137AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC, IF.
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Immunohistochemistry of paraffin-embedded human liver cancer using SOX14 Antibody at dilution of 1:1002
| Cat.No | ADC-15693A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | SOX14 |
| Target Synonyms | SOX14 antibody; SOX28 antibody; Transcription factor SOX-14 antibody; Protein SOX-28 antibody | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4 | Purification Method | >95%, Protein G purified |
| Conjugate | Non-conjugated | Application | ELISA, IF, IHC, WB |
| Storage | Upon receipt |
| Immunogen Description | Recombinant Human Transcription factor SOX-14 protein (1-137AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | O95416 |
Uniprot Id
O95416
Target Species
Human
Target Name
SOX14
Target Full Name
Transcription factor SOX-14
Target Function
Acts as a negative regulator of transcription.
Target Subcellular Location
Nucleus.
Target Synonyms
SOX14; SOX28; Transcription factor SOX-14; Protein SOX-28
Target Background
This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.
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