FAM81A Polyklonale Antilichaam, PerCP-Cy5,5 Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.
FA81B_HUMAN; FAM81B; Family with sequence similarity 81, member B; FLJ25333; Hypothetical protein LOC153643; Protein FAM81B.
145773
Cytoplasm, Nucleus
• Rabbit
281-368/368
FAM81A
• Polyclonal
• IgG
PerCP-Cy5.5
KLH conjugated synthetic peptide derived from human FAM81A
IF (IHC-P), IF (IHC-F), IF (ICC)
Purified by Protein A.
482nm/694nm
1µg/µl
IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (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.
145773
Human, Mouse, Rat
Beschrijving
FAM81A Polyklonale Antilichaam, PerCP-Cy5,5 Vervoeging Beschikbaar in 100 µL. Bestel eenvoudig online met snelle levering.
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