Anti-FAM76B Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Lieferant: Bioss
BS-9659R-A647
BOSSBS-9659R-A647EA 893 EUR
BOSSBS-9659R-A647
Anti-FAM76B Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Antikörper
With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.

Recommended Dilutions: IF(IHC-P): 1:50-200

Type: Primary
Antigen: FAM76B
Clonality: Polyclonal
Clone:
Conjugation: Alexa Fluor® 647
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat
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