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Merck

S6821

Sigma-Aldrich

Anti-SMC1L1 antibody produced in rabbit

IgG fraction of antiserum

Sinónimos:

Anti-SMC1, Anti-SMC1 structural maintenance of chromosomes 1-like 1, Anti-SMC1α

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About This Item

Número MDL:
Código UNSPSC:
12352203
NACRES:
NA.41

origen biológico

rabbit

conjugado

unconjugated

forma del anticuerpo

IgG fraction of antiserum

tipo de anticuerpo

primary antibodies

clon

polyclonal

mol peso

antigen 160 kDa

reactividad de especies

human

técnicas

immunoprecipitation (IP): 5-10 μL using 293-T cell lysates
western blot: 1:2,000-1:4,000 using extracts of HeLa nuclear cells

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

human ... SMC1A(8243)
mouse ... Smc1a(24061)
rat ... Smc1a(63996)

Descripción general

Structural maintenance of chromosomes protein 1A (SMC1A, SMC1L1, SMC1) protein belongs to the structural maintenance of chromosomes (SMC) superfamily. SMC1A gene is located on human chromosome Xp11.22.

Especificidad

Anti-SMC1L1 (also known as SMC1 and SMC1a) specifically recognizes SMC1L1.

Inmunógeno

synthetic peptide corresponding to amino acids 954-970 of human SMC1L1, conjugated to KLH via an N-terminal cysteine residue. This sequence differs from the corresponding mouse and rat sequences in 2 and 3 amino acids, respectively.

Aplicación

Anti-SMC1L1 antibody produced in rabbit may be used in immunoblotting and immunoprecipitation.

Acciones bioquímicas o fisiológicas

Structural maintenance of chromosomes protein 1A (SMC1A, SMC1L1, SMC1) protein can be phosphorylated by Ataxia-telangiectasia, mutated (ATM) indicating a potential role for this protein in DNA repair. Thus, SMC1L1 phosphorylation appears to be the critical downstream event in the ATM-nibrin (NBS1)-breast cancer type 1 (BRCA1) pathway, which mediates cell survival and chromosomal stabilization after DNA damage. Mutations in SMC1L1 gene result in the Cornelia de Lange syndrome, a multisystem developmental disorder. SMC1A protein participates in chromosome dynamics, double-strand break (DSB) repair and tumorigenesis. The gene encoding this protein can control the cell cycle and helps to maintain the stability of genome. Knockdown of SMC1A gene can block the proliferation and migration of hepatocellular carcinoma cells.

Forma física

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

Almacenamiento y estabilidad

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze 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 dilutions should be discarded if not used within 12 hours.

Cláusula de descargo de responsabilidad

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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Phosphorylation of SMC1 is a critical downstream event in the ATM-NBS1-BRCA1 pathway
Kitagawa R, et al.
Genes & Development, 18(12), 1423-1438 (2004)
Phosphorylation of SMC1A promotes hepatocellular carcinoma cell proliferation and migration
Zhang Y, et al.
International Journal of Biological Sciences, 14(9), 1081-1081 (2018)
Ilaria Parenti et al.
Epigenetics, 9(7), 973-979 (2014-04-24)
Cornelia de Lange syndrome (CdLS) is a rare multisystem disorder characterized by facial dysmorphisms, limb anomalies, and growth and cognitive deficits. Mutations in genes encoding subunits (SMC1A, SMC3, RAD21) or regulators (NIPBL, HDAC8) of the cohesin complex account for approximately

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