HAGHL Antikörper (AA 1-100) (FITC)

Produktnummer ABIN1398950

Produktdetails anti-HAGHL Antikörper (FITC)

Target: HAGHL (Hydroxyacylglutathione Hydrolase-Like (HAGHL))

Bindungsspezifität: AA 1-100

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HAGHL Antikörper ist konjugiert mit FITC

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

Kreuzreaktivität: Human, Maus

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HAGHL

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: 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 HAGHL

Target: HAGHL (Hydroxyacylglutathione Hydrolase-Like (HAGHL))

Andere Bezeichnung: HAGHL (HAGHL Produkte)

Synonyme: 1500017E18Rik antikoerper, 2810014I23Rik antikoerper, C330022E15Rik antikoerper, hydroxyacylglutathione hydrolase-like antikoerper, hydroxyacylglutathione hydrolase like antikoerper, Haghl antikoerper, HAGHL antikoerper

Hintergrund:

Synonyms: HAGHL, HAGHL_HUMAN, Hydroxyacylglutathione hydrolase-like, Hydroxyacylglutathione hydrolase-like protein.

Background: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

Gen-ID: 84264