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SAB4200542

Sigma-Aldrich

Anti-ADAR1 (C-terminal) antibody produced in rabbit

IgG fraction of antiserum

Synonym(s):

Anti-136 kDa double-stranded RNA-binding protein, Anti-DRADA, Anti-DSH, Anti-DSRAD, Anti-G1P1, Anti-IFI-4, Anti-IFI4, Anti-K88DSRBP, Anti-P136, Anti-RNA-specific, Anti-adenosine deaminase, Anti-adenosine deaminase acting on RNA 1-A, Anti-double-stranded RNA-specific adenosine deaminase, Anti-interferon-induced protein 4

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~110 kDa

species reactivity

human

technique(s)

immunoprecipitation (IP): 5-10 μL using lysates of human HepG2 or HeLa cells
western blot: 1:500-1:1000 using whole extracts of human HEK-293T or G361 cells

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... ADAR(103)

General description

Adenosine deaminase that acts in RNA (ADAR) 1 belongs to ADAR family. It is expressed in most of the human tissues. ADAR1 has several isoforms which include the full length ADAR1 (150 kDa) and two functionally active short isoforms (80 and 110 kDa).
The ADAR1 gene is mapped on the human chromosome at 1q21.3.

Specificity

Anti-ADAR1 (C-terminal) recognizes human ADAR1.

Immunogen

synthetic peptide corresponding to a sequence at the C-terminal region of human ADAR1, conjugated to KLH. The corresponding sequence is identical in rat, bovine, pig, dog and monkey and differs by one amino acid in mouse.

Application

Anti-ADAR1 (C-terminal) antibody produced in rabbit may be used in immunoblotting and immunoprecipitation.

Biochem/physiol Actions

Adenosine deaminase that acts in RNA (ADAR) facilitates RNA editing by catalyzing the hydrolytic deamination of adenosine (A) to inosine (I) in double-stranded (ds). ADAR1 plays critical roles in differentiating cells of embryo and adult tissues, facilitating cell survival and permitting their further differentiation and maturation. Its role in embryonic development is especially demonstrated within the hematopoietic lineage as well as in adult hematopoietic progenitor cells (HPCs). In addition, ADAR1 regulates hematopoietic stem cell maintenance and suppresses interferon signaling that may protect organisms from the harmful effects of interferon activation leading to various pathological conditions, such as chronic inflammation, autoimmune disorders, and cancer.

Physical form

Solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide.

Storage and Stability

For continuous use, store at 2-8 °C for up to one month. For extended storage freeze in working aliquots. Repeated freezing and thawing 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 or other company documentation accompanying the product(s), 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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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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Adenosine-to-inosine RNA editing
Zinshteyn B, et al.
Wiley Interdisciplinary Reviews. Systems Biology and Medicine, 1, 202-202 (2009)
Intracellular Localization of Differentially Regulated RNA-specific Adenosine Deaminase Isoforms in Inflammation
Yang JH, et al.
The Journal of Biological Chemistry, 278, 45833-45842 (2003)
RNA editing catalyzed by ADAR1 and its function in mammalian cells
Wang Q
Biochemistry. Biokhimiia, 76, 900-911 (2011)
Cheng-Rang Li et al.
Archives of dermatological research, 302(6), 477-480 (2010-03-20)
Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis of autosomal dominant inheritance characterized by a mixture of hyperpigmented and hypopigmented macules distributed on the dorsal aspects of the hands and feet. Genetic studies have identified mutations in ADAR1 gene to
ADAR1 is required for hematopoietic progenitor cell survival via RNA editing
XuFeng R, et al.
Proceedings of the National Academy of Sciences of the USA, 106, 17763-17768 (2009)

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