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SAB4100235

Sigma-Aldrich

Monoclonal Anti-SAMHD1 antibody produced in mouse

clone SAMHD1-A200, culture supernatant

Sinônimo(s):

AntiAGS5, AntiDCIP, AntiHD domain containing 1, AntiHDDC1, AntiMOP-5, AntiOTTHUMP00000030889, AntiSAM domain and HD domain 1, AntiSAM domain- and HD domain-containing protein 1, AntiSBBI88

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

fonte biológica

mouse

conjugado

unconjugated

forma do anticorpo

culture supernatant

tipo de produto de anticorpo

primary antibodies

clone

SAMHD1-A200, monoclonal

Formulário

aqueous solution

peso molecular

antigen predicted mol wt 72 kDa

reatividade de espécies

human

técnica(s)

western blot: suitable

Isotipo

IgG1

nº de adesão UniProt

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

Informações sobre genes

human ... SAMHD1(25939)

Descrição geral

SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 (SAMHD1) is a deoxynucleoside triphosphate triphosphohydrolase with sterile alpha motif (SAM) and a dGTP-regulated dNTP hydrolase domain (HD). SAMHD1 gene is mapped to human chromosome 20q11.23.

Imunogênio

SAMHD1 purified recombinant protein

Ações bioquímicas/fisiológicas

SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 (SAMHD1) is a key enzyme, which controls the levels of dinucleotide triphosphates. It also acts as an immune response factor cum restriction factor for many virues including the human immunodeficiency virus (HIV) hepatitis B virus (HBV) and herpes simplex virus 1 (HSV-1). SAMHD1 interferon-stimulated gene (ISG) also regulates the human cytomegalovirus and papillomavirus life cycles. Mutation in the SAMHD1 leads to imbalance in dinucleotide levels and is implicated in Aicardi‐Goutières syndrome (AGS) Mutation in SAMHD1 along with Three Prime Repair Exonuclease 1 (TREX1) and Stimulator of interferon genes (STING) genes is also correlated to familial chilblain lupus (FCL).

forma física

Solution in Dulbecco′s Modified Eagle′s Medium with 10% fetal calf serum and 15 mM sodium azide.

Exoneração de responsabilidade

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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Código de classe de armazenamento

12 - Non Combustible Liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Visite a Biblioteca de Documentos

Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus
Ravenscroft JC, et al.
American Journal of Medical Genetics. Part A, 155(1), 235-237 (2011)
SAMHD1-deficient fibroblasts from Aicardi-Goutieres Syndrome patients can escape senescence and accumulate mutations
Franzolin E, et al.
Faseb Journal, 34(1), 631-647 (2020)
SAMHD1 Regulates Human Papillomavirus 16-Induced Cell Proliferation and Viral Replication during Differentiation of Keratinocytes
James CD, et al.
mSphere, 4(4), e00448-e00419 (2019)
Microarray CGH analysis of hematological patients with del (20q)
Wu C, et al.
International Journal of Hematology, 102(5), 617-625 (2015)

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