IMPAD1 antibody (AA 81-180) (HRP)

Catalog No. ABIN716360

The Rabbit Polyclonal anti-IMPAD1 antibody is suitable to detect IMPAD1 in samples from Human. It has been validated for WB, ELISA, IHC (p) and IHC (fro).

Quick Overview for IMPAD1 antibody (AA 81-180) (HRP) (ABIN716360)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IMPAD1 antibody is conjugated to HRP

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

Product Details anti-IMPAD1 Antibody (HRP)

Binding Specificity: AA 81-180

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human IMPAD1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for IMPAD1

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

Alternative Name: IMPAD1

Background:

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.

Gene ID: 54928

Pathways: Glycosaminoglycan Metabolic Process