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The protein encoded by MAD2L2 is a component of the mitotic spindle assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. Additionally we are shipping MAD2 Mitotic Arrest Deficient-Like 2 (Yeast) Proteins (8) and many more products for this protein.
Showing 10 out of 44 products:
Human Polyclonal MAD2L2 Primary Antibody for EIA, IHC (p) - ABIN117980
Cahill, da Costa, Carson-Walter, Kinzler, Vogelstein, Lengauer: Characterization of MAD2B and other mitotic spindle checkpoint genes. in Genomics 1999
Show all 4 references for ABIN117980
Dog (Canine) Monoclonal MAD2L2 Primary Antibody for IF, WB - ABIN968795
Chen, Fang: MAD2B is an inhibitor of the anaphase-promoting complex. in Genes & development 2001
Show all 2 references for ABIN968795
Increased gonadotropins caused by the absence of functional oocytes and accumulation of DNA damage in cells caused by the lack of repair function could be responsible for the development and progression of ovarian tumors in the Rev7 mutant mouse.
the Mad2l2 (MAD2B, Rev7) gene product is not only required by PGCs, but also by pluripotent embryonic stem cells (ESCs (show NR2E3 Antibodies)), depending on the growth conditions.
results reveal an unexpected crucial function of REV7 downstream of 53BP1 in coordinating pathological DSB repair pathway choices in BRCA1-deficient cells
that MAD2B may play an important role in high glucose-mediated podocyte injury of diabetic nephropathy via modulation of Cdh1, cyclin B1, and Skp2 expression
These results demonstrated that Rev7 is essential in resolving the replication stalls caused by DNA damage during S phase.
The function of Mad2l2 is essential in PGCs, and thus of high relevance for fertility
Rev7 is essential for PGC (show PGC Antibodies) maintenance by prevention of apoptotic cell death in the mouse.
identification of the Rev7 binding surface of the Rev1 C-terminal domain
We have successfully isolated Xenopus laevis Mad2B and PRCC (show PRCC Antibodies) cDNAs, so the well-established animal model Xenopus laevis can be used as a powerful system to study in detail the role of xPRCC (show PRCC Antibodies) and xMad2B in the intricate processes of cell cycle control.
Knockdown of REV7 inhibited the migration, invasion, and epithelial-mesenchymal transition (EMT (show ITK Antibodies)) of breast cancer cells. Meanwhile, overexpression of REV7 promoted the migration, invasion, and EMT (show ITK Antibodies) of breast cancer cells.
hMAD2 also binds to the hREV7-binding sequence in hREV3 (show REV3L Antibodies), whereas hMAD2 does not bind to a similar sequence in ADAM9 (show ADAM9 Antibodies) or ELK-1 (show ELK1 Antibodies) and hREV7 does not bind to the hMAD2-binding sequence in hMAD1 or hCDC20.
data establish MAD2L2 as a crucial contributor to the control of DNA repair activity by 53BP1 (show TP53BP1 Antibodies) that promotes NHEJ by inhibiting 5' end resection downstream of RIF1 (show INSL6 Antibodies)
Rev7 is essential for mutagenesis and S phase progression in UV-irradiated fibroblasts.
These findings indicate that depletion of REV7 enhances sensitivity to cisplatin treatment in ovarian clear cell carcinoma (CCC), suggesting that REV7 is a candidate molecular target in CCC management.
MAD2L2 helps to ensure a robustly bistable switch between APC (show APC Antibodies)/C(CDC20 (show CDC20 Antibodies)) and APC (show APC Antibodies)/C(CDH1 (show CDH1 Antibodies)) during the metaphase-to-anaphase transition, thereby contributing to mitotic fidelity.
REV7 is required for anaphase-promoting complex-dependent ubiquitination and degradation of translesion DNA polymerase REV1.
MAD2B may mediate Sim2 (show SIM2 Antibodies) function during development in CNS and thereby play a critical role in pathophysiological mechanisms in Down syndrome
The protein encoded by this gene is a component of the mitotic spindle assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. The encoded protein, which is similar to MAD2L1, is capable of interacting with ADAM9, ADAM15, REV1, and REV3 proteins.
MAD2-like protein 2
, Mitotic arrest deficient 2-like protein 2
, mitotic spindle assembly checkpoint protein MAD2B
, MAD2 homolog
, mitotic arrest deficient 2-like protein 2
, Mitotic arrest defective protein 2B
, MAD2 (mitotic arrest deficient, yeast, homolog)-like 2
, REV7 homolog
, mitotic arrest deficient homolog-like 2
, polymerase (DNA-directed), zeta 2, accessory subunit