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The antibody against TBX22 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 291-520 of human TBX22 (NP_058650.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against TBX22 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 291-520 of human TBX22 (NP_058650.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-01934A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | TBX22 |
| Target Synonyms | CPX; CLPA; TBXX; ABERS; dJ795G23.1; TBX22 | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | HeLa, Mouse testis | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 291-520 of human TBX22 (NP_058650.1). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | Q9Y458 | Immunogen Sequence |
Uniprot Id
Q9Y458
Target Species
Human
Target Name
TBX22
Target Full Name
T-box transcription factor TBX22
Target Function
Probable transcriptional regulator involved in developmental processes. This is major determinant crucial to palatogenesis.
Target Involvement
Cleft palate with or without ankyloglossia, X-linked (CPX); Abruzzo-Erickson syndrome (ABERS)
Target Subcellular Location
Nucleus.
Target Tissue Specificity
Seems to be expressed at a low level.
Target Synonyms
TBX22; TBOX22; T-box transcription factor TBX22; T-box protein 22
Target Background
This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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