HEMK1 Antikörper (AbBy Fluor® 350)

Produktnummer ABIN1693291

Produktdetails anti-HEMK1 Antikörper (AbBy Fluor® 350)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HEMK1 Antikörper ist konjugiert mit AbBy Fluor® 350

Applikation: Western Blotting (WB)

Kreuzreaktivität: Maus

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HEMK1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu HEMK1

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

Andere Bezeichnung: Hemk1 (HEMK1 Produkte)

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

Hintergrund:

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

Gen-ID: 51409