MKRN3 anticorps (C-Term)

N° du produit ABIN6992123

L’anticorps anti-MKRN3 Polyclonal Lapin est utilisé pour la détection de MKRN3 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, ELISA et IF.

Aperçu rapide pour MKRN3 anticorps (C-Term) (ABIN6992123)

Antigène: MKRN3 (Makorin Ring Finger Protein 3 (MKRN3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MKRN3 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Détail du produit anti-MKRN3 anticorps

Épitope: AA 400-450, C-Term

Specificité: MKRN3 antibody is human specific. MKRN3 antibody is predicted to not cross-react with other members of the MKRN protein family.

Purification: MKRN3 antibody is affinity chromatography purified via peptide column.

Immunogène: MKRN3 antibody was raised against a 17 amino acid peptide near the carboxy terminus of human MKRN3. The immunogen is located within amino acids 400 - 450 of MKRN3.

Isotype: IgG

Information d'application

Indications d'application: MKRN3 antibody can be used for detection of MKRN3 by Western blot at 1 - 2 μ,g/mL. For immunofluorescence start at 20 μ,g/mL.

Antibody validated: Western Blot in human samples and Immunofluorescence in human samples. All other applications and species not yet tested.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: MKRN3 antibody is supplied in PBS containing 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,4 °C

Stockage commentaire: MKRN3 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.

Détails sur MKRN3

Antigène: MKRN3 (Makorin Ring Finger Protein 3 (MKRN3))

Autre désignation: MKRN3

Sujet: The Makorin ring finger 3 (MKRN3) protein contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. The MKRN3 gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome (1), but a deletion of the gene does not (2). A deficiency of MKRN3 has been shown to cause central precocious puberty in humans (3).

Poids moléculaire: Predicted: 55 kDa

Observed: 55 kDa

ID gène: 7681

NCBI Accession: NP_005655

UniProt: Q6NSB6