C9orf117 Polyklonale Antilichaam, AbBy FluorTM 594 Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
C9orf117 is a 520 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf117 maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X, Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Chromosome 9 open reading frame 117; Hypothetical protein LOC286207; CI117_HUMAN.
286207
• Rabbit
Human, Mouse, Rat
131-230/520
C9orf117
• Polyclonal
• IgG
AbBy Fluor™ 594
KLH conjugated synthetic peptide derived from human C9orf117
WB, IF
Purified by Protein A.
590nm/617nm
1µg/µl
WB (WB=1:500-2000), IF (IF=1:100-500)
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.
286207
Beschrijving
C9orf117 Polyklonale Antilichaam, AbBy FluorTM 594 Vervoeging Beschikbaar in 100 µL. Bestel eenvoudig online met snelle levering.
Specificaties
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