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C2orf27 Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501983499
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50-198-3499 100 μL
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Catalog No. 50-198-3499 Supplier Bioss Supplier No. BS15148R
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Rabbit Polyclonal Antibody

The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf27 gene product has been provisionally designated C2orf27 pending further characterization.

Specifications

Antigen C2orf27
Applications Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene C2orf27B
Gene Symbols C2orf27B
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human C2orf27.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 408029
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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