NIPA1 antibody (AA 161-260) (HRP)

Catalog No. ABIN6987628

This Rabbit Polyclonal antibody specifically detects NIPA1 in ELISA, IHC (fro) and IHC (p). It exhibits reactivity toward Human.

Quick Overview for NIPA1 antibody (AA 161-260) (HRP) (ABIN6987628)

Target: NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NIPA1 antibody is conjugated to HRP

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

Product Details anti-NIPA1 Antibody (HRP)

Binding Specificity: AA 161-260

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human NIPA1

Isotype: IgG

Application Details

Application Notes: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for NIPA1

Target: NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))

Alternative Name: NIPA1

Background:

Synonyms: FSP 3, FSP3, Magnesium transporter NIPA1, MGC102724, MGC35570, NIPA 1, NIPA1, NIPA1_HUMAN, Non imprinted in Prader Willi/Angelman syndrome region protein 1, Non-imprinted in Prader-Willi/Angelman syndrome region protein 1, Spastic paraplegia 6 (autosomal dominant), Spastic paraplegia 6 protein, SPG 6, SPG6.

Background: This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]

Gene ID: 123606

UniProt: Q7RTP0