TAPT1 rabbit pAb
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TAPT1 rabbit pAb
Background:
This gene encodes a highly conserved, putative transmembrane protein. A mutation in the mouse ortholog of this gene results in homeotic, posterior-to-anterior transformations of the axial skeleton which are similar to the phenotype of mouse homeobox C8 gene mutants. This gene is proposed to function downstream of homeobox C8 to transduce extracellular patterning information during axial skeleton development. An alternatively spliced transcript variant encoding a substantially different isoform has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]Description:
This gene encodes a highly conserved, putative transmembrane protein. A mutation in the mouse ortholog of this gene results in homeotic, posterior-to-anterior transformations of the axial skeleton which are similar to the phenotype of mouse homeobox C8 gene mutants. This gene is proposed to function downstream of homeobox C8 to transduce extracellular patterning information during axial skeleton development. An alternatively spliced transcript variant encoding a substantially different isoform has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008],UniProt:
Q6NXT6Swiss Prot:
Q6NXT6Reactivity:
Human; MouseImmunogen:
Synthesized peptide derived from human TAPT1 AA range: 295-345Clonality:
PolyclonalSource:
RabbitApplications:
WBConcentration:
1 mg/mlDilution:
WB 1:500-2000Molecular Weight:
60kDStorage Conditions:
-20°C/1 yearObserved Molecular Weight:
60kDFragment:
IgGSubcellular Location:
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Cytoplasm, cytoskeleton, cilium basal body . Membrane ; Multi-pass membrane protein .Other Product Names:
Transmembrane anterior posterior transformation protein 1 homolog (Cytomegalovirus partial fusion receptor)Gene ID (Human):
202018
