Product: TRIM24 Antibody
Catalog: AF0320
Description: Rabbit polyclonal antibody to TRIM24
Application: WB IHC IF/ICC
Cited expt.: WB, IHC
Reactivity: Human, Mouse
Prediction: Pig, Bovine, Horse, Sheep, Rabbit, Dog, Chicken
Mol.Wt.: 117kDa; 117kD(Calculated).
Uniprot: O15164
RRID: AB_2833483

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 100ul $280 In stock
 200ul $350 In stock

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Product Info

Source:
Rabbit
Application:
WB 1:500-1:3000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

Reactivity:
Human,Mouse
Prediction:
Pig(100%), Bovine(100%), Horse(100%), Sheep(100%), Rabbit(100%), Dog(100%), Chicken(100%)
Clonality:
Polyclonal
Specificity:
TRIM24 Antibody detects endogenous levels of total TRIM24.
RRID:
AB_2833483
Cite Format: Affinity Biosciences Cat# AF0320, RRID:AB_2833483.
Conjugate:
Unconjugated.
Purification:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
Storage:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
Alias:

Fold/Unfold

E3 ubiquitin protein ligase TRIM24; E3 ubiquitin-protein ligase Trim24; hTIF1; PTC6; RING finger protein 82; RNF82; TF1A; TIF1; TIF1-alpha; TIF1A; TIF1A_HUMAN; TIF1ALPHA; Transcription intermediary factor 1-alpha; Transcriptional intermediary factor 1 alpha; Transcriptional intermediary factor 1; Trim24; Tripartite motif containing 24; Tripartite motif-containing protein 24;

Immunogens

Immunogen:

A synthesized peptide derived from human TRIM24, corresponding to a region within C-terminal amino acids.

Uniprot:
Gene(ID):
Description:
TRIM24 an atypical protein kinase that functions as a transcriptional coactivator. Originally identified as a mammalian protein that enhances the AF-2 activity of the retinoid X receptor (RXR) in a yeast genetic screen. Binds to nuclear receptors in an agonist and AF2-activating domain (AF2-AD) dependent manner. Binding to the agonist-nuclear receptor complex induces its own hyperphosphorylation as well as the phosphorylation of TFIIEa, TAFII28, and TAFII55.
Sequence:
MEVAVEKAVAAAAAASAAASGGPSAAPSGENEAESRQGPDSERGGEAARLNLLDTCAVCHQNIQSRAPKLLPCLHSFCQRCLPAPQRYLMLPAPMLGSAETPPPVPAPGSPVSGSSPFATQVGVIRCPVCSQECAERHIIDNFFVKDTTEVPSSTVEKSNQVCTSCEDNAEANGFCVECVEWLCKTCIRAHQRVKFTKDHTVRQKEEVSPEAVGVTSQRPVFCPFHKKEQLKLYCETCDKLTCRDCQLLEHKEHRYQFIEEAFQNQKVIIDTLITKLMEKTKYIKFTGNQIQNRIIEVNQNQKQVEQDIKVAIFTLMVEINKKGKALLHQLESLAKDHRMKLMQQQQEVAGLSKQLEHVMHFSKWAVSSGSSTALLYSKRLITYRLRHLLRARCDASPVTNNTIQFHCDPSFWAQNIINLGSLVIEDKESQPQMPKQNPVVEQNSQPPSGLSSNQLSKFPTQISLAQLRLQHMQQQVMAQRQQVQRRPAPVGLPNPRMQGPIQQPSISHQQPPPRLINFQNHSPKPNGPVLPPHPQQLRYPPNQNIPRQAIKPNPLQMAFLAQQAIKQWQISSGQGTPSTTNSTSSTPSSPTITSAAGYDGKAFGSPMIDLSSPVGGSYNLPSLPDIDCSSTIMLDNIVRKDTNIDHGQPRPPSNRTVQSPNSSVPSPGLAGPVTMTSVHPPIRSPSASSVGSRGSSGSSSKPAGADSTHKVPVVMLEPIRIKQENSGPPENYDFPVVIVKQESDEESRPQNANYPRSILTSLLLNSSQSSTSEETVLRSDAPDSTGDQPGLHQDNSSNGKSEWLDPSQKSPLHVGETRKEDDPNEDWCAVCQNGGELLCCEKCPKVFHLSCHVPTLTNFPSGEWICTFCRDLSKPEVEYDCDAPSHNSEKKKTEGLVKLTPIDKRKCERLLLFLYCHEMSLAFQDPVPLTVPDYYKIIKNPMDLSTIKKRLQEDYSMYSKPEDFVADFRLIFQNCAEFNEPDSEVANAGIKLENYFEELLKNLYPEKRFPKPEFRNESEDNKFSDDSDDDFVQPRKKRLKSIEERQLLK

Predictions

Predictions:

Score>80(red) has high confidence and is suggested to be used for WB detection. *The prediction model is mainly based on the alignment of immunogen sequences, the results are for reference only, not as the basis of quality assurance.

Species
Results
Score
Pig
100
Horse
100
Bovine
100
Sheep
100
Dog
100
Chicken
100
Rabbit
100
Xenopus
0
Zebrafish
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

Research Backgrounds

Function:

Transcriptional coactivator that interacts with numerous nuclear receptors and coactivators and modulates the transcription of target genes. Interacts with chromatin depending on histone H3 modifications, having the highest affinity for histone H3 that is both unmodified at 'Lys-4' (H3K4me0) and acetylated at 'Lys-23' (H3K23ac). Has E3 protein-ubiquitin ligase activity. Promotes ubiquitination and proteasomal degradation of p53/TP53. Plays a role in the regulation of cell proliferation and apoptosis, at least in part via its effects on p53/TP53 levels. Up-regulates ligand-dependent transcription activation by AR, GCR/NR3C1, thyroid hormone receptor (TR) and ESR1. Modulates transcription activation by retinoic acid (RA) receptors, including RARA. Plays a role in regulating retinoic acid-dependent proliferation of hepatocytes (By similarity).

PTMs:

Sumoylated.

Subcellular Location:

Nucleus. Cytoplasm.
Note: Colocalizes with sites of active transcription. Detected both in nucleus and cytoplasm in some breast cancer samples. Predominantly nuclear.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location

References

1). E3 ubiquitin ligase TRIM24 deficiency promotes NLRP3/Caspase‐1/IL‐1β‐mediated pyroptosis in endometriosis. CELL BIOLOGY INTERNATIONAL, 2021 (PubMed: 33724611) [IF=3.3]

Application: WB    Species: Human    Sample: ectopic endometrial tissues

FIGURE 1 The expression of tripartite motif‐containing 24 (TRIM24) was decreased in ectopic endometrial tissues. (a) The expression of TRIM24 in the normal endometrium (NE) and ectopic endometrium of endometriosis (EMS) was detected by immunohistochemistry (IHC). Representative IHC images are shown. Scale bar=50μm; (b) TRIM24 protein expression was measured by Western blot analysis in NE and EMS. The data are expressed as means±SD. GAPDH, glyceraldehyde 3‐phosphate dehydrogenase. *p<.05 by two‐tailed Student's t test

Application: IHC    Species: Human    Sample: ectopic endometrial tissues

FIGURE 3 TRIM24 negatively regulated pyroptosis and cell migration of hESC. (a, b) The transfection efficiency of TRIM24 using TRIM24‐small‐interfering RNA (siTRIM24) or TRIM24‐pcDNA3.1 (TRIM24 over ) was detected by real‐time polymerase chain reaction (a) and Western blot analysis (b); (c) representative Western blots of TRIM24 and pyroptotic proteins; (d, e) the quantitative comparison of protein expression; (f, g) the supernatant concentrations of IL‐1β and IL‐18 were tested by enzyme‐linked immunosorbent assay; (h) after being transfected with siTRIM24, the migration of normal hESC was measured by Transwell migration assay; (i) after being transfected with TRIM24‐ pcDNA3.1 (TRIM24 over ), the migration of ectopic hESC was detected by Transwell migration assay. Scale bar=100 μm. NC represents negative control groups. The data are expressed as means±SD. GAPDH, glyceraldehyde 3‐phosphate dehydrogenase; hESC, human endometrial stromal cell; IL, interleukin; TRIM24, tripartite motif‐containing 24. **p<.01 and ***p<.001 by one‐way analysis of variance with Bonferroni's multiple comparison tests

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