| Overview |
| bs-17406R-BF555 |
| phospho-HIRA (Thr555) Polyclonal Antibody, AbBy Fluor-555 Conjugated |
| WB |
| Human, Mouse |
| Rat, Dog, Cow, Sheep, Pig, Horse, Rabbit |
| Specifications |
| AbBy Fluor-555 |
| Rabbit |
| KLH conjugated synthesised phosphopeptide derived from human HIRA around the phosphorylation site of Thr555 |
| Thr555 |
| Polyclonal |
| IgG |
| 1ug/ul |
| Purified by Protein A. |
| Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Store at -20C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles. |
| Target |
| 7290 |
| P54198 |
| Nucleus |
| HIRA (phospho T555); p-HIRA (phospho T555); DGCR1;
DGGR 1;
DGGR1;
DiGeorge critical region gene 1;
HIR;
HIR histone cell cycle regulation defective homolog A;
HIRA;
HIRA protein;
HIRA_HUMAN;
Protein HIRA;
TUP 1;
TUP1;
TUP1 like enhancer of split protein 1;
TUP1-like enhancer of split protein 1;
TUPLE 1;
TUPLE1. |
| This gene encodes a histone chaperone that preferentially places the variant histone H3.3 in nucleosomes. Orthologs of this gene in yeast, flies, and plants are necessary for the formation of transcriptionally silent heterochomatin. This gene plays an important role in the formation of the senescence-associated heterochromatin foci. These foci likely mediate the irreversible cell cycle changes that occur in senescent cells. It is considered the primary candidate gene in some haploinsufficiency syndromes such as DiGeorge syndrome, and insufficient production of the gene may disrupt normal embryonic development. [provided by RefSeq, Jul 2008]
|
| Application Dilution |
| WB |
|
Powered by Bioz