Date published: 2026-2-14

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FLJ35848 Inhibitors

FLJ35848, based on its nomenclature, is likely one of the proteins identified during large-scale genomic and transcriptomic studies. The "FLJ" designation is often used for human proteins that were initially identified through such efforts, but whose detailed biological roles and functions have not been completely characterized. As with many proteins labeled with the "FLJ" prefix, the specific cellular roles, interactions, and significance of FLJ35848 might not be fully elucidated. However, the mere identification and sequencing of such proteins offer a foundation upon which further functional studies can be built, thereby unraveling their biological importance over time. The specific domains, motifs, or structural features of FLJ35848 could provide preliminary insights into its potential roles or interactions within the cell.

Inhibitors targeting FLJ35848 would represent a class of molecules specifically tailored to modulate the activity, function, or stability of FLJ35848. Considering the potential limited understanding of the exact roles of FLJ35848, inhibitory molecules would serve dual purposes: they could act as tools to modulate its activity and also as probes to help elucidate its biological function. Potential inhibitors might include small molecules that bind directly to FLJ35848, disrupting its native function or interfering with its interactions with other cellular components. These interactions, when modulated, could shed light on the protein's role in cellular processes. Another avenue of inhibition could involve molecules that affect the post-translational modifications of FLJ35848, potentially influencing its activity, cellular localization, or its interactions with other proteins. Through the study of FLJ35848 inhibition, insights can be gleaned into its cellular roles, contributions to physiological processes, and its interactions within the intricate web of cellular components and pathways.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

Actinomycin D binds to DNA, inhibiting RNA polymerase and thus transcription of many genes.

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$41.00
$84.00
$275.00
127
(6)

Cycloheximide inhibits the translational elongation step in protein synthesis, reducing protein levels.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

A DNA methyltransferase inhibitor, it can alter gene expression patterns across the cell.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

By inhibiting mTOR, rapamycin affects protein synthesis and can reduce levels of many proteins.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

An inhibitor of histone deacetylase, potentially affecting gene expression across the cell.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$269.00
$1050.00
26
(2)

An RNA polymerase II inhibitor, it can halt transcription of many genes.

I-BET 151 Hydrochloride

1300031-49-5 (non HCl Salt)sc-391115
10 mg
$450.00
2
(0)

An inhibitor of the BET family of bromodomain proteins, affecting transcription.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

A JNK inhibitor, potentially affecting various signaling pathways and subsequent gene expression.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

Another MEK inhibitor, potentially affecting various signaling pathways and subsequent gene expression.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

A proteasome inhibitor, affecting protein degradation and potentially overall protein levels.