SAMD9L anticorps (AA 1223-1557) (Fluoro488)

N° du produit ABIN8042754

L’anticorps anti-SAMD9L Polyclonal Lapin est utilisé pour la détection de SAMD9L dans des échantillons de Humain. Il a été validé pour FACS.

Aperçu rapide pour SAMD9L anticorps (AA 1223-1557) (Fluoro488) (ABIN8042754)

Antigène: SAMD9L (Sterile alpha Motif Domain Containing 9-Like (SAMD9L))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SAMD9L est conjugé à/à la Fluoro488

Application: Flow Cytometry (FACS)

Détail du produit anti-SAMD9L anticorps (Fluoro488)

Épitope: AA 1223-1557

Fonction: Anti-SAMD9L Antibody Fluoro488 Conjugated

Réactivité croisée (Details): No cross reactivity with other proteins.

Homologie: Human SAMD9L shares 69.3% amino acid (aa) sequence identity with mouse SAMD9L,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human SAMD9L recombinant protein (Position: L1223-R1557). Human SAMD9L shares 69.3% amino acid (aa) sequence identity with mouse SAMD9L, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur SAMD9L

Antigène: SAMD9L (Sterile alpha Motif Domain Containing 9-Like (SAMD9L))

Autre désignation: SAMD9L

Sujet:

Background: This gene encodes a cytoplasmic protein that acts as a tumor suppressor but also plays a key role in cell proliferation and the innate immune response to viral infection. The encoded protein contains an N-terminal sterile alpha motif domain. Naturally occurring mutations in this gene are associated with myeloid disorders such as juvenile myelomonocytic leukemia, acute myeloid leukemia, and myelodysplastic syndrome. Naturally occurring mutations are also associated with hepatitis-B related hepatocellular carcinoma, normophosphatemic familial tumoral calcinosis, and ataxia-pancytopenia syndrome.

Gene Full Name: sterile alpha motif domain containing 9 like

ID gène: 219285

UniProt: Q8IVG5