TBX15 Antibodies

AND TBX15 ELISA kits, TBX15 Proteins

Many biological assays use antibodies to detect TBX15, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with TBX15 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop TBX15 antibodies...

We validate the specificity of these antibodies to TBX15 by testing them on tissues known to express TBX15 positively and negatively. Browse below to find the TBX15 antibody that suites your experiment. We have 1 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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TBX15 Infographic by Boster Bio

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TBX15 (NM_152380) Human Over-expression Lysate

Human

$960
Cat # LS006913
20 µg, 100 µg

TBX15 Overview

Facts about T-box transcription factor TBX15.

TBX15 3D structure. Source: alphafold

T-box transcription factor TBX15 (TBX15)

Probable transcriptional regulator involved in the development of the skeleton of the limb, vertebral column and mind. Acts by controlling the amount of mesenchymal precursor cells and chondrocytes (By similarity).

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Gene Information

Human
Gene Name:	TBX15
Uniprot:	Q96SF7
Entrez:	6913

Family

Belongs to:

No superfamily

Alternative Names

T-box 14; T-box 15; T-box protein 14; T-box protein 15; T-box transcription factor TBX14; T-box transcription factor TBX15; TBX14

Molecular Weight

Mass (kDA):
65.757 kDA

Genomic Context


Human

Location:	1p12
Sequence:	1; NC_000001.11 (118883046..118989510, complement)

Subcellular Localizations

Nucleus.

Diseases

Obesity
Ulnar-mammary Syndrome Of Pallister
Diabetes Mellitus
Metabolic Diseases
Holt-oram Syndrome
Craniofacial Abnormalities
Congenital Anomaly Of Skeletal Bone
Pre-eclampsia
Fetal Growth Retardation
Thick Lips And Oral Mucosa
Malignant Neoplasms
Neoplasms

Placenta Disorders
Dwarfism
Malignant Neoplasm Of Prostate
Hereditary Diseases
Obesity, Abdominal
Congenital Abnormality

Interacting Proteins

ATXN1
POLE2
VENTX

Pathways

Pigmentation
Mesoderm Formation
Methylation
Segmentation
Cell Proliferation
Gland Development
Somitogenesis
Dna Methylation
Larval Development
Mammary Gland Development
Ossification
Localization

Limb Development
Somite Development
Paraxial Mesoderm Formation
Flight
Histone Acetylation
Bone Development

PTMs

Methylation

Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/TBX15

References

PMID: 19068278 by Lausch E., et al. TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome.