HAGHL anticorps (AA 1-100) (Cy7)

N° du produit ABIN1416818

Détail du produit anti-HAGHL anticorps (Cy7)

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

Épitope: AA 1-100

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

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

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

Réactivité croisée: Humain, Souris

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human HAGHL

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 HAGHL

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

Autre désignation: HAGHL (HAGHL Produits)

Synonymes: anticorps 1500017E18Rik, anticorps 2810014I23Rik, anticorps C330022E15Rik, anticorps hydroxyacylglutathione hydrolase-like, anticorps hydroxyacylglutathione hydrolase like, anticorps Haghl, anticorps HAGHL

Sujet:

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.

ID gène: 84264