NPAP1 Polyklonale Antilichaam, RBITC Vervoeging

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.

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

23742

Q9NZP6

Nucleus

Human

801-900/1156

NPAP1

RBITC

KLH conjugated synthetic peptide derived from human NPAP1

WB, IF (IHC-P)

Purified by Protein A.

570nm/595nm

1µg/µl

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

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

Unmodified

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

23742