Anti-KMT1B / SUV39H2 antibody - C-terminal
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(1 Publication)
Rabbit Polyclonal KMT1B / SUV39H2 antibody. C-terminal. Suitable for WB and reacts with Mouse, Human samples. Cited in 1 publication. Immunogen corresponding to Recombinant Fragment Protein within Human SUV39H2 aa 100-350.
View Alternative Names
KMT1B, SUV39H2, Histone-lysine N-methyltransferase SUV39H2, Histone H3-K9 methyltransferase 2, Lysine N-methyltransferase 1B, Suppressor of variegation 3-9 homolog 2, H3-K9-HMTase 2, Su(var)3-9 homolog 2
- WB
Supplier Data
Western blot - Anti-KMT1B / SUV39H2 antibody - C-terminal (AB189842)
Blocking buffer : 3% nonfat dry milk in TBST.
All lanes:
Western blot - Anti-KMT1B / SUV39H2 antibody - C-terminal (ab189842) at 1/1000 dilution
Lane 1:
SW620 cell lysate at 25 µg
Lane 2:
MCF-7 cell lysate at 25 µg
Lane 3:
U-937 cell lysate at 25 µg
Lane 4:
293T cell lysate at 25 µg
Lane 5:
HeLa cell lysate at 25 µg
Lane 6:
Mouse heart tissue lysate at 25 µg
Lane 7:
Mouse liver tissue lysate at 25 µg
Lane 8:
Mouse eye tissue lysate at 25 µg
Secondary
All lanes:
HRP Goat Anti-Rabbit IgG (H+L)
Predicted band size: 47 kDa
false
Reactivity data
Properties and storage information
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Shipped at conditions
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Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This protein influences epigenetic constructs by being part of the transcriptional repressor complex. It is involved in gene silencing through the formation of heterochromatin an essential process for maintaining genome stability. KMT1B shares homology with SUV39H1 another histone methyltransferase and both cooperate in establishing heterochromatin markers.
Pathways
KMT1B participates in the transcriptional regulation pathway and intersects with pathways governing cell cycle control. It contributes to the E2F transcriptional repression pathway by interacting with retinoblastoma protein (pRB) which controls cell proliferation. This connection to pRB positions KMT1B as an influential factor in cell cycle checkpoints and progression.
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Target data
Publications (1)
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Frontiers in cell and developmental biology 9:778345 PubMed35096813
2022
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
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