NPAP1 Polyklonale Antilichaam, Cy7 Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
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
• Rabbit
Human
801-900/1156
NPAP1
• Polyclonal
• IgG
Cy7
KLH conjugated synthetic peptide derived from human NPAP1
WB, IF (IHC-P)
Purified by Protein A.
743nm/767nm
1µg/µl
WB (1:300-5000), IF (IHC-P) (1:50-200)
Aqueous buffered solution containing 0.01M TBS (pH 7.4) 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
Beschrijving
NPAP1 Polyklonale Antilichaam, Cy7 Vervoeging Beschikbaar in 20 µL. Bestel eenvoudig online met snelle levering.
Specificaties
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