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Browse our anti-Homeobox D13 (HOXD13) Antibodies

Full name:
anti-Homeobox D13 Antibodies (HOXD13)
On www.antibodies-online.com are 73 Homeobox D13 (HOXD13) Antibodies from 18 different suppliers available. Additionally we are shipping Homeobox D13 Proteins (5) and many more products for this protein. A total of 86 Homeobox D13 products are currently listed.
Synonyms:
B230397M16Rik, BDE, BDSD, Hox-4.8, HOX4I, hoxd-13, hoxd13, nmf11, oscillator, ot, SP-D, spasmodic, SPD, spdh, XHoxd13, zgc:110511
list all antibodies Gene Name GeneID UniProt
HOXD13 14654  
HOXD13 288154  
HOXD13 3239 P35453

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Top referenced anti-Homeobox D13 Antibodies

  1. Human Polyclonal HOXD13 Primary Antibody for EIA, WB - ABIN952786 : Salsi, Ferrari, Ferraresi, Cossarizza, Grande, Zappavigna: HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by geminin. in Molecular and cellular biology 2009 (PubMed)
    Show all 4 references for ABIN952786

  2. Human Polyclonal HOXD13 Primary Antibody for ELISA, IHC - ABIN4319735 : Cantile, Franco, Tschan, Baumhoer, Zlobec, Schiavo, Forte, Bihl, Liguori, Botti, Tornillo, Karamitopoulou-Diamantis, Terracciano, Cillo: HOX D13 expression across 79 tumor tissue types. in International journal of cancer 2009 (PubMed)

More Antibodies against Homeobox D13 Interaction Partners

Zebrafish Homeobox D13 (HOXD13) interaction partners

  1. Data show that cis (show CISH Antibodies)-regulatory elements driving Hoxd gene expression in distal limbs are present in fish.

Mouse (Murine) Homeobox D13 (HOXD13) interaction partners

  1. The age-associated accumulation of somatic mutations that occurs in the Nup98 (show NUP98 Antibodies)-HOXD13 (NHD13) mouse model of leukemia progression was significantly elevated by co-expression of a PKR (show EIF2AK2 Antibodies) transgene.

  2. Shox2 (show SHOX2 Antibodies) expression restricted to the proximal limb along with Hoxd9 (show HOXD9 Antibodies) and Hoxa11 (show HOXA11 Antibodies) expression, juxtaposing the distal expression of Hoxa13 (show HOXA13 Antibodies) and Hoxd13.

  3. Data indicate that loss of cyclin-dependent kinase inhibitor p15 (p15Ink4b (show CDKN2B Antibodies)) collaborates with oncogene (show RAB1A Antibodies) fusion protein Nup98 (show NUP98 Antibodies)-HoxD13 transgene in the development of predominantly myeloid neoplasms.

  4. study elucidated the mechanism underlying a novel missense mutation in HOXD13 (Q317K) associated with a complex hand and foot malformation phenotype; results show that the mutation results in a shift in the binding profile of the mutant toward a bicoid/PITX1 (show PITX1 Antibodies) motif

  5. providing synpolydactyly limb explant cultures with cells expressing either HOXD13 or WNT5A (show WNT5A Antibodies) led to a non-cell autonomous partial rescue of cell polarity the perichondral region and restored the expression of perichondral markers.

  6. a slight and transient deregulation of Hoxd13 expression can readily affect the relative lengths of limb segments during development

  7. Mutation of a zinc-binding residue in the glycine receptor (show GLRB Antibodies) alpha1 changes ethanol sensitivity in vitro and alcohol consumption in Glra1 (show GLRA1 Antibodies)(D80A) knock-in mice.

  8. TM3 (show TPM1 Antibodies)-4 loop subdomains are important for functional reconstitution of glycine receptors by independent domains

  9. findings show that expression of NUP98 (show NUP98 Antibodies)-HOXD13 impairs class switch recombination and reduces the antibody-mediated immune response, in addition to its role in leukemia

  10. Mice expressing both the FLT3 (show FLT3 Antibodies)/ITD and Nup98 (show NUP98 Antibodies)-HoxD13 (NHD13) fusion gene developed acute myeloid leukemia (show BCL11A Antibodies) with 100% penetrance

Human Homeobox D13 (HOXD13) interaction partners

  1. a novel mutation causing truncation of HOXD13 protein was successfully identified as being associated with an atypical non-syndromic SPD phenotype in our study.

  2. down-regulation of HOXD13 might be a potentially useful prognostic marker for patients with breast cancer.

  3. A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation.

  4. HOXD13 methylation is a common event in primary breast cancer and is associated with poor survival of breast cancer patients.

  5. A 27 bp expansion mutation in exon 1 of HOXD13 was associated with autosomal dominant synpolydactyly in a Chinese family.

  6. Linkage analysis of the syndactyly type 1 subtype c (SD1-c) phenotype based on two Chinese families with 3/4 fingers syndactyly shows that two missense mutations in codon 306 of HOXD13 underlie SD1-c.

  7. Identification of a novel c.659G>C (p.Gly220Ala) mutation outside the HOXD13 homeodomain responsible for synpolydactyly in a Chinese family.

  8. A genome-wide array-comparative genomic hybridization (aCGH) analysis revealed global chromosomal aberration in MWCNTs-treated clones, predominantly at chromosome 2q31-32, where the potential oncogenes HOXD9 (show HOXD9 Antibodies) and HOXD13 are located

  9. Data indicate increased levels of reactive oxygen species (ROS (show ROS1 Antibodies)) were detected in bone marrow nucleated cells (BMNC) that express CD71 (show TFRC Antibodies) in in NUP98 (show NUP98 Antibodies)-HOXD13 (NHD13) transgenic mice, a murine model for myelodysplastic syndromes (MDS (show PAFAH1B1 Antibodies)).

  10. Molecular characteristics of a HOXD13 synpolydactyly 1 nonsense mutation in a Chinese family.

Homeobox D13 (HOXD13) Antigen Profile

Antigen Summary

This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.

Alternative names and synonyms associated with Homeobox D13 (HOXD13)

  • homeobox D13 (HOXD13) antibody
  • homeobox D13 (hoxd13) antibody
  • homeobox D13 (LOC100218824) antibody
  • homeo box D13a (hoxd13a) antibody
  • glycine receptor, alpha 1 subunit (Glra1) antibody
  • homeo box D13 (Hoxd13) antibody
  • homeobox D13 (Hoxd13) antibody
  • surfactant protein D (Sftpd) antibody
  • B230397M16Rik antibody
  • BDE antibody
  • BDSD antibody
  • Hox-4.8 antibody
  • HOX4I antibody
  • hoxd-13 antibody
  • hoxd13 antibody
  • nmf11 antibody
  • oscillator antibody
  • ot antibody
  • SP-D antibody
  • spasmodic antibody
  • SPD antibody
  • spdh antibody
  • XHoxd13 antibody
  • zgc:110511 antibody

Protein level used designations for anti-Homeobox D13 (HOXD13) Antibodies

homeobox D13 , homeobox gene D-13 , glycine receptor 48 kDa subunit , glycine receptor strychnine-binding subunit , glycine receptor subunit alpha-1 , homeobox protein Hox-D13 , homeo box 4I , homeo box D13 , homeobox protein Hox-4I , homeobox protein Hox-4.8 , chox-4.8 , chox-4G , homeobox protein Hox-4G , homeobox protein hoxd13 , CP4 , PSP-D , lung surfactant protein D , pulmonary surfactant protein D , pulmonary surfactant-associated protein D , surfactant associated protein D , surfactant, pulmonary-associated protein D

GENE ID SPECIES
100301549 Oryctolagus cuniculus
399207 Xenopus laevis
470586 Pan troglodytes
100218824 Taeniopygia guttata
100271866 Felis catus
30407 Danio rerio
14654 Mus musculus
288154 Rattus norvegicus
3239 Homo sapiens
520424 Bos taurus
15433 Mus musculus
396415 Gallus gallus
100152793 Sus scrofa
25350 Rattus norvegicus
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