NPAP1 Polyclonal Antibody, APC Conjugated

Product Specifications

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.

Synonyms

NPAP1; NPAP 1; NPAP-1; Nuclear pore associated protein 1; NPAP1_HUMAN; C15orf2.

Gene ID

23742

Swiss Prot

Q9NZP6

Cellular Locus

Nucleus

Host

Rabbit

Cross Reactivity

Human

Immunogen

801-900/1156

Target

NPAP1

Clonality

Polyclonal

Conjugation

APC

Source

KLH conjugated synthetic peptide derived from human NPAP1

Applications

WB, IF (IHC-P)

Purification

Purified by Protein A.

Excitation Emission

650nm/660nm

Concentration

1ug/ul

Dilution

WB (1:300-5000), IF (IHC-P) (1:50-200)

Buffer

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Modification

Unmodified

Storage Conditions

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

Gene ID URL

23742

Isotype

IgG

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