NPAP1 antibody (AA 800-850)

Catalog No. ABIN1385442

This anti-NPAP1 antibody is a Rabbit Polyclonal antibody detecting NPAP1 in WB, IF (p) and IHC (p). Suitable for Human.

Quick Overview for NPAP1 antibody (AA 800-850) (ABIN1385442)

Target: NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NPAP1 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-NPAP1 Antibody

Binding Specificity: AA 800-850

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human NPAP1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for NPAP1

Target: NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))

Alternative Name: NPAP1

Background:

Synonyms: NPAP1, NPAP 1, NPAP-1, Nuclear pore associated protein 1, NPAP1_HUMAN, C15orf2.

Background: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.

Gene ID: 23742

UniProt: Q9NZP6