recommended for detection of SETD4 of mouse and human origin by WB, IP and ELISA; also reactive with additional species, including canine
Modification Notes
SETD4 (SET domain-containing protein 4) is a 440 amino acid protein that contains one SET domain and is expressed as three isoforms produced by alternative splicing. The gene that encodes SETD4 maps to human chromosome 21. The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
WB:1:500~1:2000 IP:1:100~1:500 Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of SETD4 of mouse and human origin by WB IP and ELISA also reactive with additional species including canine
Tissue Specificity
recommended for detection of SETD4 of mouse and human origin by WB, IP and ELISA; also reactive with additional species, including canine