TXNL4A anticorps (AA 1-142)

N° du produit ABIN6149737

Détail du produit anti-TXNL4A anticorps

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

Épitope: AA 1-142

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TXNL4A est non-conjugé

Application: Western Blotting (WB)

Séquence: MSYMLPHLHN GWQVDQAILS EEDRVVVIRF GHDWDPTCMK MDEVLYSIAE KVKNFAVIYL VDITEVPDFN KMYELYDPCT VMFFFRNKHI MIDLGTGNNN KINWAMEDKQ EMVDIIETVY RGARKGRGLV VSPKDYSTKY RY

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human TXNL4A (NP_006692.1).

Isotype: IgG

Information d'application

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

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

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 (TXNL4A Produits)

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

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.,TXNL4A,BMKS,DIB1,DIM1,SNRNP15,TXNL4,U5-15kD,Cell Biology & Developmental Biology,Apoptosis,TXNL4A

Poids moléculaire: 16 kDa

ID gène: 10907

UniProt: P83876

Pathways: Ribonucleoprotein Complex Subunit Organization