C16orf57 anticorps (N-Term)

N° du produit ABIN5517969

Cet anticorps Lapin Polyclonal détecte spécifiquement C16orf57 dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour C16orf57 anticorps (N-Term) (ABIN5517969)

Antigène: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C16orf57 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-C16orf57 anticorps

Épitope: N-Term

Fonction: USB1 Antibody - N-terminal region

Séquence: LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP80076-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur C16orf57

Antigène: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Autre désignation: USB1

Sujet:

Background Information: This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

Gene Name: U6 snRNA biogenesis phosphodiesterase 1

Alternative Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57

Protein Name: U6 snRNA phosphodiesterase

Poids moléculaire: 20 kDa

ID gène: 79650

NCBI Accession: NP_001182231

UniProt: Q9BQ65