KC-6630

293T-MLLT1-HiBiT-KI Cell Line

65475

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Background of 293T-MLLT1-HiBiT-KI Cell Line

MLLT1 (MLLT1 super elongation complex subunit), also known as ENL or YEATS1, is a nuclear protein and core component of the super elongation complex (SEC) that plays a critical role in transcriptional regulation. The gene is located on chromosome 19p13.3 and encodes a 559-amino acid protein containing an evolutionarily conserved YEATS domain, an ANC1 homology domain, and intrinsically disordered regions. As an epigenetic "reader," MLLT1 recognizes acetylated and crotonylated lysine residues on histone H3 via its YEATS domain, thereby facilitating transcription elongation by RNA polymerase II and recruitment of chromatin remodeling complexes . MLLT1 is ubiquitously expressed in human tissues and is essential for embryonic development, as demonstrated by the embryonic lethality of Mllt1 knockout mice prior to 8.5 days post-coitum.

Specifications

Catalog Number	KC-6630
Cell Line Name	293T-MLLT1-HiBiT-KI Cell Line
Clone Number	1B1
Host Cell Line	293T
Description	Stable 293T cell clone expressing endogenous C-terminal HiBiT tagged MLLT1
Quantity	Two vials of frozen cells (≥2-10⁶/vial)
Stability	Stable in culture over a minimum of 10 passages
Application	Drug screening and biological assays
Freezing Medium	70% DMEM+20% FBS+10% DMSO
Propagation Medium	DMEM+10%FBS
Selection Marker	NA
Morphology	Epithelial
Subculture	Split saturated culture 1:3-1:6 every 2-3 days; seed out at about 1-3 × 10⁵ cells/mL
Incubation	37 °C with 5% CO₂
Storage	Liquid nitrogen immediately upon receiving
Doubling Time	Approximately 30 hours
Mycoplasma Status	Negative

Cell Line Generation

293T-MLLT1-HiBiT-KI cell line was generated using the CRISPR method.

Characterization

Figure 1: Characterization of 293T-MLLT1-HiBiT-KI cell line stable clone using PCR sequencing.

Figure 2: Characterization of 293T-MLLT1-HiBiT-KI cell line stable clone using RT-PCR sequencing.

Figure 3. Characterization of HiBiT degradation by MLLT1 Degrader.

Cell Resuscitation

Prewarm culture medium (DMEM+10%FBS)in a 37°C water bath.
Thaw the frozen vial in a 37°C water bath for 1-2 minutes.
Transfer the vial into biosafety cabinet, and wipe the surface with 70% ethanol.
Unscrew the top of the vial and transfer the cell suspension gently into a sterile centrifuge tube containing 9.0mL complete culture medium.
Spin at ~ 125 × g for 5-7 minutes at room temperature, and discard the supernatant without disturbing the pellet.
Resuspend cell pellet with the appropriate volume of complete medium and transfer the cell suspension into a T25 culture flask.
Incubate the flask at 37°C, 5% CO₂ incubator.
Split saturated culture 1:3-1:6 every 2-3 days; seed out at about 1-3 × 10⁵ cells/mL.

Cell Freezing

Prepare the freezing medium (70% DMEM+20% FBS+10% DMSO) fresh immediately before use.
Keep the freezing medium on ice and label cryovials.
Transfer cells to a sterile, conical centrifuge tube, and count the cells.
Centrifuge the cells at 250×g for 5 minutes at room temperature and carefully aspirate off the medium.
Resuspend the cells at a density of at least 3×10⁶ cells/mL in chilled freezing medium.
Aliquot 1 mL of the cell suspension into each cryovial.
Freeze cells in the CoolCell freezing container overnight in a -80°C freezer.
Transfer vials to liquid nitrogen for long-term storage

References

Nie Z, et al. (2003). "Novel SWI/SNF chromatin-remodeling complexes contain a mixed-lineage leukemia chromosomal translocation partner." Molecular and Cellular Biology, 23(8), 2942-2952.
Kabra A, Bushweller J. (2022). "The intrinsically disordered proteins MLLT3 (AF9) and MLLT1 (ENL) - multimodal transcriptional switches with roles in normal hematopoiesis, MLL fusion leukemia, and kidney cancer." Journal of Molecular Biology, 434(1), 167117.

Use License Agreement

Research Use Only.

Not for use in diagnostic procedures or therapeutic applications.

Redistribution of the cell line or its derivatives is prohibited without prior written permission from Kyinno Biotechnology.