TXNL4A Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2734686

Détail du produit

Antigène: TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette TXNL4A protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human TXNL4A / DIM1 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

Antigène: TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Autre désignation: Txnl4a,dim1 (TXNL4A Produits)

Synonymes: Txnl4 Protein, TXNL4A Protein, txnl4a Protein, dim1 Protein, MGC85128 Protein, DIB1 Protein, DIM1 Protein, HsT161 Protein, SNRNP15 Protein, TXNL4 Protein, U5-15kD Protein, D18Wsu98e Protein, Dim1 Protein, ENSMUSG00000057130 Protein, U5-15kDa Protein, thioredoxin-like 4A Protein, thioredoxin like 4A Protein, thioredoxin like 4A S homeolog Protein, Txnl4a Protein, TXNL4A Protein, txnl4a Protein, LOC664328 Protein, txnl4a.S Protein

Sujet: The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 16.6 kDa

NCBI Accession: NP_006692

Pathways: Ribonucleoprotein Complex Subunit Organization