DCUN1D4 anticorps (AA 161-270) (Alexa Fluor 488)

N° du produit ABIN1398070

Détail du produit anti-DCUN1D4 anticorps (Alexa Fluor 488)

Antigène: DCUN1D4 (DCN1, Defective in Cullin Neddylation 1, Domain Containing 4 (DCUN1D4))

Épitope: AA 161-270

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DCUN1D4 est conjugé à/à la Alexa Fluor 488

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Souris

Homologie: Human,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human DCUN1D4

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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, 0.03 % 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 DCUN1D4

Antigène: DCUN1D4 (DCN1, Defective in Cullin Neddylation 1, Domain Containing 4 (DCUN1D4))

Autre désignation: DCUN1D4 (DCUN1D4 Produits)

Synonymes: anticorps RGD1310422, anticorps si:ch211-14g4.1, anticorps AI836376, anticorps DCN1-like protein 4, anticorps defective in cullin neddylation 1 domain containing 4, anticorps DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae), anticorps LOC100282616, anticorps LOC100283419, anticorps dcnl4, anticorps DCUN1D4, anticorps Dcun1d4, anticorps dcun1d4

Sujet:

Synonyms: DCN1, defective in cullin neddylation 1, domain containing 4, DCN1 like protein 4, DCUN1 domain containing protein 4, DCUN1D 4, KIAA0276, DCNL4_HUMAN.

Background: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

ID gène: 23142