epitope mapping near the N-terminus of SETD4 of human origin
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
WBIPIFELISA
recommended for detection of SETD4 of mouse, rat and human origin by WB, IP, IF and ELISA non cross-reactive with isoforms A, B or 3:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping near the N-terminus of SETD4 of human origin
Tissue Specificity
epitope mapping near the N-terminus of SETD4 of human origin