SMC1-a antibody (pAb)

Host / Isotype

Rabbit / IgG

Reactivity

Human

Applications

ChIP-Seq, IP, WB

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Cat No : 61067,61068 61067

Synonyms

SMC, SMC1, DNA damage, phosphorylation, ATM, double strand break, cohesin, Structural Maintenance of Chromosomes, cell cycle, antibody, antibodies, polyclonal, serine, phospho-serine, sample, western blotting, wb, immunoprecipitation, ip



Product Information

Tested Applications ChIP-Seq, IP, WB

Applications Validated by Active Motif: ChIP-Seq: 4 ug (7 ul) per ChIP IP: 10 ul per IP WB*: 1:1,000 - 1:5,000 dilution *Note: many chromatin-bound proteins are not soluble in a low salt nuclear extract and fractionate to the pellet. Therefore, we recommend a High Salt / Sonication Protocol when preparing nuclear extracts for Western blot.

Tested Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen This SMC-a antibody was raised against a peptide within the C-terminal region of human SMC1-a.
Full Name SMC1-a antibody (pAb)
Synonyms SMC, SMC1, DNA damage, phosphorylation, ATM, double strand break, cohesin, Structural Maintenance of Chromosomes, cell cycle, antibody, antibodies, polyclonal, serine, phospho-serine, sample, western blotting, wb, immunoprecipitation, ip
Molecular weight 160 kDa
GenBank accession numberNP_006297
RRIDAB_2688006
Purification Method Affinity Purified
Buffer Purified IgG in 70 mM Tris (pH 8), 105 mM NaCl, 31 mM glycine, 0.07 mM EDTA, 30% glycerol and 0.035% sodium azide. Sodium azide is highly toxic.
Storage Some products may be shipped at room temperature. This will not affect their stability or performance. Avoid repeated freeze/thaw cycles by aliquoting items into single-use fractions for storage at -20°C for up to 2 years. Keep all reagents on ice when not in storage.

Background Information

The Structural Maintenance of Chromosomes (SMC) family proteins play critical roles in various nuclear events that require structural changes of chromosomes, including mitotic chromosome organization, DNA recombination and repair and global transcriptional repression. SMC1 has a myosin-like ATPase domain that serves as a molecular motor to help organize chromatin and is part of the cohesin complex that facilitates chromosome cohesion during the cell cycle. SMC1 and SMC3 form a heterodimeric complex required for metaphase progression in mitotic cells. SMC1 is also involved in DNA damage repair. Subsequent to double strand DNA breaks, SMC1 is phosphorylated by the ATM kinase. Phosphorylated SMC1 is crucial to the successful repair of DNA damage. Defects in SMC1 isoform A are the cause of Cornelia de Lange syndrome type 2, an inherited developmental disorder associated with malformations affecting multiple systems.