SMYD2A anticorps (Cy7)

N° du produit ABIN715577

L’anticorps anti-SMYD2A Polyclonal Lapin est utilisé pour la détection de SMYD2A dans des échantillons de Humain. Il a été validé pour WB et IF.

Aperçu rapide pour SMYD2A anticorps (Cy7) (ABIN715577)

Antigène: SMYD2A (SET and MYND Domain Containing 2a (SMYD2A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SMYD2A est conjugé à/à la Cy7

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

Détail du produit anti-SMYD2A anticorps (Cy7)

Fonction: SMYD2 Polyclonal Antibody, Cy7 Conjugated

Réactivité croisée: Souris, Rat

Homologie: Human,Dog,Cow,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SMYD2

Isotype: IgG

Information d'application

Indications d'application: WB(1:500-2000), IF(1:100-500)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur SMYD2A

Antigène: SMYD2A (SET and MYND Domain Containing 2a (SMYD2A))

Autre désignation: SMYD2

Sujet:

Synonyms: HSKM B, HSKM-B, HSKMB, Histone methyltransferase SMYD2, HSKM-B, Lysine N-methyltransferase 3C, MGC119305, N lysine methyltransferase SMYD2, N-lysine methyltransferase SMYD2, SET and MYND domain containing 2, SET and MYND domain containing protein 2, SET and MYND domain-containing protein 2, Smyd2, SMYD2_HUMAN, Zinc finger MYND domain containing 14, ZMYND14.

Background: This gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008]

ID gène: 56950

UniProt: Q9NRG4