特徴
- 主な研究分野例:Cell Biology
- 背景:C16orf45, also known as FLJ32618, is a 204 amino acid protein encoded by a gene mapping to human chromosome 16. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
仕様
- サイズ:60uL
- 抗体タイプ:Polyclonal Antibody
- アプリケーション:IHC,ELISA
- 交差性:Human, Mouse, Rat
- 宿主:Rabbit
- アイソタイプ:IgG
- 濃度:0.7 mg/mL
- 抗原:Synthetic peptide of human C16orf45
- 緩衝液:PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
- 精製方法:Antigen affinity purification
- 希釈倍率:IHC 1:30-1:150, ELISA 1:5000-1:10000
- 標識:Unconjugated
- クローナリティ:Polyclonal
- メーカーマニュアルリンク:https://www.elabscience.com/viewpdf-253749-Elabscience-E-AB-17744.pdf
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商品のバリエーション (サイズ違い・スペック違い・オプション品など)
| 商品イメージ | アズワン品番 商品名 |
|---|---|
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89-7835-57
C16orf45 Polyclonal Antibody 200uL
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89-7835-54
C16orf45 Polyclonal Antibody 20uL
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89-7835-55
C16orf45 Polyclonal Antibody 60uL
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89-7835-56
C16orf45 Polyclonal Antibody 120uL
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