IMPAD1 anticorps (AA 81-180) (HRP)

N° du produit ABIN716360

L’anticorps anti-IMPAD1 Polyclonal produit chez le Lapin a été validé pour WB, ELISA, IHC (p) et IHC (fro). Il convient pour la détection de IMPAD1 dans des échantillons provenant de Humain. }

Aperçu rapide pour IMPAD1 anticorps (AA 81-180) (HRP) (ABIN716360)

Antigène: IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IMPAD1 est conjugé à/à la HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-IMPAD1 anticorps (HRP)

Épitope: AA 81-180

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human IMPAD1

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

Conseil sur la manipulation: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 IMPAD1

Antigène: IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))

Autre désignation: IMPAD1

Sujet:

Synonyms: IMP 3, IMPA3, IMPase 3, Inositol monophosphatase domain containing protein 1, Myo inositol monophosphatase A3.

Background: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

ID gène: 54928

Pathways: Glycosaminoglycan Metabolic Process