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Anti-Propionyl-Histone H3 (Lys23) Rabbit pAb
Catalog Number: PTM-205
$ 435

Clone Number: /

Host: Rabbit Clonality: Polyclonal

Applications： WB IHC-P ChIP

Reactivity: Human, Mouse, Rat

Synonyms: H3K23pr

Product Size
100 μl
Quantity

Shipping: Ambient temperature

Order online or send purchase order to info@ptmbio.com

FAQ Technical Support Protocols

General Information
Isotype IgG
Conjugate Unconjugated
Synonyms H3K23pr
UniProt ID

P68431

Immunogen Propionylated human histone H3 (Lys23) peptide
MW (kDa) 15
Specificity Anti-Propionyl-Histone H3 (Lys23) Rabbit pAb detects histone H3 only when it is propionylated at Lys23.
Product Usage Information
Applications Dilution Recommended Species
WB 1:500 - 1:2000 Human, Mouse, Rat
IHC-P 1:200 - 1:1000 Human, Rat
ChIP 6μg per 5x106 cells Human
Properties
Purity Protein A and immunogen affinity purified
Constituents PBS, Glycerol, BSA
Storage Store at -20°C. Avoid freeze/thaw cycles.
Stability Stable for 12 months from date of receipt/reconstitution.
Target Information

Background

Histones are subject to a variety of enzyme-catalyzed modifications, including acetylation, methylation, phosphorylation, ubiquitylation, and others. Among these modifications, lysine propionylation (Kpr) has emerged as a newly identified reversible modification that plays a crucial role in controlling protein activity. Structurally similar to lysine acetylation, lysine propionylation is prevalent in both prokaryotes and eukaryotes and has been identified in a wide range of proteins, including histones and non-histone substrates like p53. Recent research has unveiled the involvement of stoichiometric complexes comprising lysine acetyltransferase 6A (KAT6A), KAT6B, and bromodomain- and PHD finger-containing protein 1 (BRPF1) in the catalysis of histone H3 Lys23 propionylation (H3K23pr). Importantly, deficiencies in histone propionylation have been associated with developmental disorders and cancer.

Cellular location

Nucleus

Images
Dot Blot

Peptide amount: 1ng, 4 ng, 16 ng
Blocking buffer: 5% NFDM/TBST
Primary Ab dilution: 1:2000
Primary Ab incubation condition: 2 hours at room temperature
Secondary Ab: Goat Anti-Rabbit IgG H&L pAb (HRP Conjugate)
Exposure time: 60 seconds
The list of peptides used in the experiment is provided below.
Lane 1: H3K23 propionyl. Lane 2: H3K18 acetyl.
Lane 3: H3K23 acetyl. Lane 4: H3K23 butyryl.
Lane 5: H3K23 crotonyl. Lane 6: H3K27 acetyl.
Lane 7: H3K27 butyryl. Lane 8: H3K23 unmodified.
WB

Lysates: (-): HeLa cells; (+): HeLa cells treated with 10 mM sodium propionate for 4 hours
Protein loading amount: 20 μg
Blocking buffer: 5% NFDM/TBST
Primary Ab dilution: 1:2000
Primary Ab incubation condition: 2 hours at room temperature
Secondary Ab: Goat Anti-Rabbit IgG H&L pAb (HRP Conjugate)
Exposure time: 60 seconds
Predicted band size: 15 kDa
Observed band size: 17 kDa
IHC-P

Tissue: Human spleen
Section type: Formalin fixed & paraffin-embedded section
Retrieval method: High temperature and high pressure
Retrieval buffer: Tris/EDTA buffer, pH 9.0
Primary Ab dilution: 1:200
Primary Ab incubation condition: 1 hour at room temperature
Secondary Ab: Anti-Rabbit and Mouse Polymer HRP (Ready to Use)
Counter stain: Hematoxylin (blue)
Description: The brown color represents the positive signal observed with PTM-205.

Tissue: Rat stomach
Section type: Formalin fixed & paraffin-embedded section
Retrieval method: High temperature and high pressure
Retrieval buffer: Tris/EDTA buffer, pH 9.0
Primary Ab dilution: 1:1000
Primary Ab incubation condition: 1 hour at room temperature
Secondary Ab: Anti-Rabbit and Mouse Polymer HRP (Ready to Use)
Counter stain: Hematoxylin (blue)
Description: The brown color represents the positive signal observed with PTM-205.
ChIP

Sample: HeLa cells treated with 10 mM sodium propionate for 4 hours
Cross-linking conditions: No cross-linking
Amount of chromatin per IP: 5×106 cells
Amount of Ab per IP: 6 μg
Beads type and amount per IP: 50 μL of Protein A MagBeads
Description: Chromatin immunoprecipitations were performed with 6 μg of normal rabbit IgG as a negative control. The immunoprecipitated DNA was quantified by real-time PCR using primers specific for the human GAPDH CDS, RPL30 exon 3, LDHA, FOXO3a promoter, FOXO3a downstream, RAB20, TUBBP10, and LDHA promoter regions. The data are presented as enrichment of each sample relative to total amount of input chromatin at each amplicon.

Research Use

For research use only, not for use in diagnostic procedures.

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