IMPAD1 antibody (AA 81-180) (Biotin)

Catalog No. ABIN716353

Product Details anti-IMPAD1 Antibody (Biotin)

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

Binding Specificity: AA 81-180

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IMPAD1 antibody is conjugated to Biotin

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

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.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for IMPAD1

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

Alternative Name: IMPAD1 (IMPAD1 Products)

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

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