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In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Additionally we are shipping HOXA2 Antibodies (32) and HOXA2 Proteins (8) and many more products for this protein.
Hoxa2 knockdown in Xenopus results in hyoid to mandibular homeosis.
The role of HOXA2 gene in dominant isolated microtia and the dysmorphogenetic effect of this gene on ear development
5 genomic variants in GSC (show GSC ELISA Kits), HOXA2 and PRKRA (show PRKRA ELISA Kits) were identified through mutational analysis in Chinese patients with microtia.
The Hoxa2-mediated decay of RCHY1 (show RCHY1 ELISA Kits) involves both the 19S and 20S proteasome (show PSMA5 ELISA Kits) complexes
HOXA2 acts as a suppressor or TBP (show TBP ELISA Kits)-antagonist to inhibit MMP-9 (show MMP9 ELISA Kits) expression; while methylation-mediated inactivation of HOXA2 in NPC (show NPC1 ELISA Kits) derepresses MMP-9 (show MMP9 ELISA Kits) production and increases invasion of NPC (show NPC1 ELISA Kits) cells.
we have identified a nonsense mutation (Q235*) in HOXA2 that segregates with bilateral nonsyndromic microtia and hearing loss through three generations of a family in an autosomal dominant pattern.
Lack of mutations in the coding region of HOXA2 among the sporadic microtia patients.
A missense mutation in the HOXA2 in a consanguineous iranian family with bilateral microtia was reported.
Hoxa2, Meis and Pbx proteins act cooperatively on the ECR, via a core 32 bp sequence, to regulate Hmx1 (show HMX1 ELISA Kits) expression.
our data support that KPC2 regulates Hoxa2 by promoting its relocation to the cytoplasm.
Ectopic Hoxa2 expression results in the transformation of the proximal Meckel's cartilage and the malleus into a supernumerary styloid process (SP), a second pharyngeal arch-derived mammalian-specific skeletal structure.
Hoxa2 operates as a tissue-specific cofactor, enhancing Meis binding to specific sites that provide the second arch with its anatomical identity
The impairment of chondrogenic differentiation by Hoxa2 overexpression.
Data show that the transcription factor Hoxa2 binds to Pcp4 chromatin and regulates Pcp4 expression in the second arch.
Hoxa2 partly controls the morphogenesis of the pinna through the BMP signalling pathway and expression of Eya1 (show EYA1 ELISA Kits), which in humans is involved in branchio-oto (show PGAP1 ELISA Kits)-renal syndrome.
Hoxb2 (show HOXB2 ELISA Kits) antagonizes Hoxa2 during rostral hindbrain oligodendrogenesis.
the sustained expression of Hoxa2 in the chondrocyte lineage is characterized by a proportionate short stature resulting from skeletal growth defect.
The data reveals that Hoxa2 has large genome coverage and potentially regulates thousands of genes.
In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. The encoded protein may be involved in the placement of hindbrain segments in the proper location along the anterior-posterior axis during development.
homeobox protein Hox-1K
, homeobox protein Hox-A2
, homeobox A2
, homeobox A1
, homeo box A1
, homeo box A2
, homeobox protein Hox-1.11
, transcription factor Hoxa2b
, transcription factor Hoxa2
, Homeobox protein Hox-A2
, homeobox protein Hox-A2-like
, Homeobox gene A11
, Homeobox gene A2
, Homeobox protein Hox-1.11
, homeo box A2b
, homeobox gene A-2
, homeobox protein Hox-A2b