biological source
mouse
conjugate
unconjugated
antibody form
purified from hybridoma cell culture
antibody product type
primary antibodies
clone
ADAR2-15, monoclonal
form
buffered aqueous solution
mol wt
antigen ~130 kDa
species reactivity
human
technique(s)
western blot: 1:250-1:500 using HEK-293T cells overexpressing ADAR2 (a working dilution)
isotype
IgG
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... ADAR2(104)
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General description
Adenosine deaminase acting on RNA type 2 (ADAR2), also known as adenosine deaminase, RNA specific B1 (ADARB1), is encoded by the gene mapped to human chromosome 21q22.3. ADARB1 is characterized with two double-stranded RNA-binding domains and a deaminase domain involved in editing action.
Monoclonal Anti-ADAR2 (mouse IgG2a isotype) is derived from the hybridoma ADAR2-15 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide corresponding to a fragment of human ADAR2, conjugated to KLH. Adenosine deaminase acting on RNA type 2 is expressed mainly in nucleus.
Application
Monoclonal Anti-ADAR2 antibody produced in mouse may be used in several immunochemical techniques including immunoblotting.
Biochem/physiol Actions
Adenosine deaminase acting on RNA type 2 (ADAR2) enzyme plays a vital role in editing pre-mRNA of glutamate receptor B subunit. Combined effect of ADAR2 and HTR2C (5-hydroxytryptamine receptor 2C) variants contribute to the suicide attempt (SA) vulnerability in psychiatric patients. ADAR2 is a candidate gene for neurological diseases, such as bipolar affective disorder and epilepsy. Decrease in the activity of ADAR2 enzyme results in α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor-mediated death of motor neurons in mice. ADAR2 enzyme is expressed consistently in carcinomas and sarcomas and it is upregulated in lymphomas and seminomas when compared to normal tissues.
Monoclonal Anti-ADAR2 recognizes human ADAR2
Physical form
Solution in 0.01M phosphate buffered saline pH 7.4, containing 15 mM sodium azide and horse immunoglobulins
Preparation Note
Store at −20 °C. For continuous use, store at 2–8 °C for up to one month. For extended storage, freeze at −20 °C in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.
Disclaimer
Unless otherwise stated in our catalog, our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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存储类别
12 - Non Combustible Liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
常规特殊物品
此项目有
SUMO-1 modification alters ADAR1 editing activity
Desterro JMP
Molecular Biology of the Cell, 16(11), 5115-5126 (2005)
Sequence analysis of ADARB1 gene in patients with familial bipolar disorder.
Amore M
Journal of Affective Disorders, 81, 79-85 (2004)
Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disorders.
Karanovic J
The World Journal of Biological Psychiatry : The Official Journal of the World Federation of Societies of Biological Psychiatry, 16, 261-271 (2015)
Genomics screen in transformed stem cells reveals RNASEH2A, PPAP2C, and ADARB1 as putative anticancer drug targets.
Flanagan JM
Molecular Cancer Therapeutics, 8, 249-260 (2009)
Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3.
Mittaz L
Genomics, 41, 210-217 (1997)
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