IMPAD1 anticorps (AA 81-180) (Biotin)

N° du produit ABIN716353

Détail du produit anti-IMPAD1 anticorps (Biotin)

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

Épitope: AA 81-180

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

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

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

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.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur IMPAD1

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

Autre désignation: IMPAD1 (IMPAD1 Produits)

Synonymes: anticorps IMP 3, anticorps RGD1306455, anticorps gPAPP, anticorps impa3, anticorps 1110001C20Rik, anticorps AA408880, anticorps AI451589, anticorps AL022796, anticorps B230207P20, anticorps Jaws, anticorps GPAPP, anticorps IMP-3, anticorps IMPA3, anticorps IMPase 3, anticorps zgc:123256, anticorps inositol monophosphatase domain containing 1, anticorps inositol monophosphatase domain containing 1 S homeolog, anticorps Impad1, anticorps impad1.S, anticorps IMPAD1, anticorps 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