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| Cat.No | ACP12638 | Target Name | ESS2 |
|---|---|---|---|
| Form | Lyophilized powder | Expression System | Custom Production. Please inquire and provide the desire expression system. |
| Expression Range | 1-476 | Protein Length | Full length protein |
| Purity | >85% (SDS-PAGE) | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q96DF8 |
|---|
Uniprot Id
Q96DF8
Target Species
Human
Target Name
ESS2
Target Full Name
Splicing factor ESS-2 homolog
Target Function
May be involved in pre-mRNA splicing.
Target Subcellular Location
Nucleus.
Target Protein Families
ESS2 family
Target Tissue Specificity
Highly expressed in heart, brain and skeletal muscle. Detected at low levels in placenta.
Target Synonyms
DGC14_HUMAN; DGCR13; DGCR14; DGS H; DGS I; DGS-H; DGSH; DGSI; DiGeorge syndrome critical region 13; DiGeorge syndrome critical region 14; DiGeorge syndrome critical region gene 14; DiGeorge syndrome critical region gene DGSI; DiGeorge syndrome critical region protein 14; DiGeorge syndrome gene H; DiGeorge syndrome gene I; DiGeorge syndrome protein H; ES2; ES2 protein ; Es2el; Protein DGCR14; Protein ES2
Target Background
This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene.
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