epitope mapping near the C-terminus of FAM109B of human origin
Modification Notes
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The FAM109B gene product has been provisionally designated FAM109B pending further characterization.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of FAM109B of mouse, rat and human origin by WB, IP, IF and ELISA also reactive with additional species, including bovine and porcine:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping near the C-terminus of FAM109B of human origin
Tissue Specificity
epitope mapping near the C-terminus of FAM109B of human origin
Western blot analysis of FAM109B expression in HeLa (A), MCF7 (B), K-562 (C) and A-10 (D) whole cell lysates.
Application
Western blot analysis of FAM109B expression in mouse heart tissue extract.
Application Notes
recommended for detection of FAM109B of mouse, rat and human origin by WB, IP, IF and ELISA also reactive with additional species, including bovine and porcine:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.