HEMK1 anticorps (AA 21-120)

N° du produit ABIN1714060

Détail du produit anti-HEMK1 anticorps

Antigène: HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))

Épitope: AA 21-120

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HEMK1 est non-conjugé

Application: Western Blotting (WB), ELISA

Réactivité croisée: Souris

Homologie: Human,Rat,Dog,Cow,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human HEMK1

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur HEMK1

Antigène: HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))

Autre désignation: HEMK1 (HEMK1 Produits)

Synonymes: anticorps HEMK, anticorps MTQ1, anticorps 2310008M14Rik, anticorps AW049265, anticorps RGD1308293, anticorps HemK methyltransferase family member 1, anticorps CpipJ_CPIJ016651, anticorps HEMK1, anticorps Hemk1

Sujet:

Synonyms: HEMK, HemK methyltransferase family member 1, Hemk1, HEMK1_HUMAN, M.HsaHemKP, MTQ1.

Background: HEMK1 is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. name change

ID gène: 51409