SETMAR anticorps (Internal Region)

N° du produit ABIN6287089

Détail du produit anti-SETMAR anticorps

Antigène: SETMAR (SET Domain and Mariner Transposase Fusion Gene (SETMAR))

Épitope: Internal Region

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SETMAR est non-conjugé

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Fonction: Rabbit polyclonal to SETMAR.

Specificité: SETMAR Polyclonal Antibody detects endogenous levels of SETMAR protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from human SETMAR.

Isotype: IgG

Information d'application

Indications d'application: IHC 1:100-1:300
ELISA 1:40000

Commentaires:

Widely expressed, with highest expression in placenta and ovary and lowest expression in skeletal muscle.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: Store at -20°C, and avoid repeat freeze-thaw cycles.

Détails sur SETMAR

Antigène: SETMAR (SET Domain and Mariner Transposase Fusion Gene (SETMAR))

Autre désignation: SETMAR (SETMAR Produits)

Synonymes: anticorps HsMar1, anticorps METNASE, anticorps Mar1, anticorps 5830404F24Rik, anticorps Etet2, anticorps SETMAR, anticorps zgc:172212, anticorps SET domain and mariner transposase fusion gene, anticorps SET domain without mariner transposase fusion, anticorps histone-lysine N-methyltransferase SETMAR, anticorps SETMAR, anticorps Setmar, anticorps LOC470738, anticorps setmar, anticorps LOC703880, anticorps LOC100447656, anticorps LOC100586616

Poids moléculaire: 76.669 kDa

ID gène: 6419

UniProt: Q53H47

Pathways: Positive Regulation of Response to DNA Damage Stimulus