TBX22 Antibodies

AND TBX22 ELISA kits, TBX22 Proteins

Many biological assays use antibodies to detect TBX22, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with TBX22 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop TBX22 antibodies...

We validate the specificity of these antibodies to TBX22 by testing them on tissues known to express TBX22 positively and negatively. Browse below to find the TBX22 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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TBX22 Infographic by Boster Bio

All TBX22 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-TBX22 Antibody

7 Q&As

Human

$360
Cat # A06861
100 µl

Anti-TBX22 (A30) Antibody

Human, Mouse, Rat

IHC, WB

$405
Cat # A06861-1
100ul

TBX22 Overview

Facts about T-box transcription factor TBX22.

TBX22 3D structure. Source: alphafold

T-box transcription factor TBX22 (TBX22)

Probable transcriptional regulator involved in developmental processes. This is major determinant crucial to palatogenesis.

Gene Information

Human
Gene Name:	TBX22
Uniprot:	Q9Y458
Entrez:	50945

Family

Belongs to:

No superfamily

Alternative Names

cleft palate and/or ankyloglossia; CLPA; CPX; dJ795G23.1; T-box 22; T-box protein 22; T-box transcription factor TBX22; TBOX22; TBXX

Molecular Weight

Mass (kDA):
57.91 kDA

Genomic Context


Human

Location:	Xq21.1
Sequence:	X; NC_000023.11 (80014753..80031774)

Tissue Specificity

Seems to be expressed at a low level.

Subcellular Localizations

Nucleus.

Diseases

Cleft Palate
Tongue Tie
Cleft Palate, X-linked
Cleft Lip
Cleft Palate With Cleft Lip
Congenital Abnormality
Tongue Diseases
Hypodontia
Genetic Diseases, X-linked
Dysplasia
Neoplasms
Dysequilibrium Syndrome

Submucous Cleft Of Hard Palate
Craniofacial Abnormalities
Developmental Absence Of Tooth
Pterygium
Rosselli-gulienetti Syndrome
Atresia
Malignant Tumor Of Colon

Interacting Proteins

VENTX

Pathways

Pathogenesis
Palate Development
Localization
Cell Proliferation
Mating
Ossification
Conjugation

Tongue Development

PTMs

Sumoylation

Research Areas

Stem Cell Markers

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/TBX22

References

PMID: 11024289 by Laugier-Anfossi F., et al. Molecular characterization of a new human T-box gene (TBX22) located in Xq21.1 encoding a protein containing a truncated T-domain.

PMID: 11559848 by Braybrook C., et al. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.