TXNL4A anticorps

N° du produit ABIN6566788

Cet anticorps Lapin Polyclonal détecte spécifiquement TXNL4A dans WB. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour TXNL4A anticorps (ABIN6566788)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TXNL4A est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-TXNL4A anticorps

Purification: Affinity purification

Immunogène: Recombinant protein of human TXNL4A

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur TXNL4A

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

Autre désignation: TXNL4A

Sujet:

Synonyms: BMKS,DIB 1,DIB1,DIM 1,DIM1,DIM1 protein homolog,HsT161,SNRNP15,Spliceosomal U5 snRNP specific 15 kDa protein,Spliceosomal U5 snRNP-specific 15 kDa protein,Thioredoxin like 4,Thioredoxin like 4A,Thioredoxin like protein 4A,Thioredoxin like U5 snRNP protein U5 15kD,Thioredoxin-like protein 4A,Thioredoxin-like U5 snRNP protein U5-15kD,TXN4A,TXNL 4,TXNL 4A,TXNL4,txnl4a,U5 15kD

Background: 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:

Observed_MW: 13kDa

Calculated_MW: 16kDa

ID gène: 10907

UniProt: P83876

Pathways: Ribonucleoprotein Complex Subunit Organization