Homeobox protein Hox-D13 Antibodies

AND HOXD13 ELISA kits, Homeobox protein Hox-D13 Proteins

Many biological assays use antibodies to detect Homeobox protein Hox-D13, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Homeobox protein Hox-D13 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Homeobox protein Hox-D13 antibodies...

We validate the specificity of these antibodies to Homeobox protein Hox-D13 by testing them on tissues known to express HOXD13 positively and negatively. Browse below to find the HOXD13 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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HOXD13 Infographic by Boster Bio

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Anti-Homeobox protein Hox-D13 HOXD13 Antibody

Human, Mouse, Rat

$405
Cat # A03000
100ul

HOXD13 Overview

Facts about Homeobox protein Hox-D13.

HOXD13 3D structure. Source: alphafold

Homeobox protein Hox-D13 (HOXD13)

Sequence-specific transcription factor that binds gene promoters and activates their transcription (PubMed:24789103). Part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis (By similarity).

Gene Information

Human
Gene Name:	HOXD13
Uniprot:	P35453
Entrez:	3239

Family

Belongs to:

Abd-B homeobox family

Alternative Names

BDSD; homeo box 4I; homeo box D13; homeobox D13; Homeobox protein Hox-4I; homeobox protein Hox-D13; HOX4IBDE; SPD

Molecular Weight

Mass (kDA):
36.101 kDA

Genomic Context


Human

Location:	2q31.1
Sequence:	2; NC_000002.12 (176087487..176095944)

Subcellular Localizations

Nucleus.

Diseases

Syndactyly
Limb Deformities, Congenital
Polydactyly
Leukemia
Congenital Hand Deformities
Leukemia, Myelocytic, Acute
Myeloid Leukemia
Brachydactyly
Congenital Foot Deformity
Congenital Abnormality
Chromosomal Translocation

Malignant Neoplasms
Neoplasms
Haploinsufficiency
Cell Transformation, Neoplastic
Hypoplasia
Trinucleotide Repeat Expansion

Pathways

Limb Development
Pathogenesis
Limb Morphogenesis
Ossification
Localization
Cell Death
Cell Differentiation
Cell Proliferation
Fin Development
Programmed Cell Death
Fertilization
Embryo Development
Reverse Transcription

Translation
System Development
Cell Cycle
Regionalization
Genitalia Development
Methylation
Nervous System Development

PTMs

Methylation

Cleavage

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/HOXD13

References

PMID: 8614804 by Muragaki Y., et al. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13.

PMID: 1675198 by D'Esposito M., et al. EVX2, a human homeobox gene homologous to the even-skipped segmentation gene, is localized at the 5' end of HOX4 locus on chromosome 2.