recommended for detection of RNase HII-A of human origin by WB, IP, IF, IHC(P) and ELISA
Modification Notes
The RNase HII complex is an endonuclease that degrades RNA found in RNA:DNA duplexes and is composed of one catalytic subunit and two non-catalytic subunits. RNase HII-A, also called RNASEH2A (Ribonuclease H2 subunit A), RNASEHI, AGS4 or RNHIA, is the 299 amino acid catalytic subunit of RNase HII. Localized to the nucleus, RNase HII-A mediates the removal of Okazaki fragment RNA primers that are present on the lagging strand during DNA replication. RNase HII-A catalyzes the endonucleolytic cleavage of RNA to a 5’-phosphomonoester and is able to bind magnesium or manganese as cofactors. Defects in the gene encoding RNase HII-A are the cause of Aicardi-Goutieres syndrome type 4 (AGS4), an autosomal recessive encephalopathy characterized by cerebral atrophy, leukodystrophy, intracranial calcifications and chronic cerebrospinal fluid (CSF) lymphocytosis. Patients affected by AGS4 have severe neurological dysfunctions and often die in early childhood.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFIHCELISA
WB:1:500~1:2000 IP:1:100~1:500 IF:1:200~1:500 IHC:1:50~1:200 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 RNase HII-A of human origin by WB IP IF IHC(P) and ELISA
Tissue Specificity
recommended for detection of RNase HII-A of human origin by WB, IP, IF, IHC(P) and ELISA