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Anti-Crotonyl-Histone H3 (Lys9) Mouse mAb
Catalog Number: PTM-539
$ 435

Clone Number: /

Host: Mouse Clonality: Monoclonal

Applications： WB ChIP

Reactivity: Human, Mouse, Rat

Synonyms: H3K9cr

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 H3K9cr
UniProt ID

P68431

Immunogen Crotonylated human histone H3 (Lys9) peptide
MW (kDa) 15
Specificity Anti-Crotonyl-Histone H3 (Lys9) Mouse mAb detects histone H3 only when it is crotonylated at Lys9.
Product Usage Information
Applications Dilution Recommended Species
WB 1:500 - 1:2000 Human, Mouse, Rat
ChIP 6 μg per 5x106 cells Human
Properties
Purity Protein G 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, etc. Crotonylation of lysine is a newly identified reversible modification controlling chromosome structure and gene transcription. The reversible lysine crotonylation has been well demonstrated in eukaryotic histones from worm to human. The unique structure and genomic localization of histone lysine crotonylation suggest that it is mechanistically and functionally different from histone lysine acetylation. Specifically, in both human somatic and mouse male germ cell genomes, histone crotonylation marks either active promoters or potential enhancers. Crotonylation of histone H3 at Lys9 may play a vital role in the epigenetic modulation, including chromatin remodeling and DNA transcriptional regulation.

Cellular location

Nucleus

Images
Dot Blot

Peptide amount: 1 ng, 4 ng, 16 ng
Blocking buffer: 5% NFDM/TBST
Primary Ab dilution: 1:1000
Primary Ab incubation: 2 hours at room temperature
Secondary Ab: Goat Anti-Mouse IgG H&L pAb (HRP Conjugate)
Exposure time: 60 seconds
The list of peptides used in the experiment is provided below.
Lane 1: H3K9 crotonyl. Lane 2: H3K4 acetyl.
Lane 3: H3K4 butyryl. Lane 4: H3K4 crotonyl.
Lane 5: H3K4 2-hydroxyisobutyryl. Lane 6: H3K4 β-hydroxybutyryl.
Lane 7: H3K9 acetyl. Lane 8: H3K9 butyryl.
Lane 9: H3K9 2-hydroxyisobutyryl. Lane 10: H3K9 β-hydroxybutyryl.
Lane 11: H3K14 acetyl. Lane 12: H3K14 propionyl.
Lane 13: H3K14 butyryl. Lane 14: H3K14 succinyl.
Lane 15: H3K14 crotonyl. Lane 16: H3K14 2-hydroxyisobutyryl.
Lane 17: H3K14 β-hydroxybutyryl. Lane 18: H3K9 unmodified.
WB

Lysates: (-): HeLa cells; (+): HeLa cells treated with 100 ng/ml crotonic acid for 18 hours
Protein loading amount: 20 μg
Blocking buffer: 5% NFDM/TBST
Primary Ab dilution: 1:2000
Primary Ab incubation: 2 hours at room temperature
Secondary Ab: Goat Anti-Mouse IgG H&L pAb (HRP Conjugate)
Exposure time: 60 seconds
Predicted band size: 15 kDa
Observed band size: 15 kDa
ChIP

Sample: HeLa cells treated with 10 mM crotonic acid for 15 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/G MagBeads
Description: Chromatin immunoprecipitations were performed with 6 μg of normal mouse IgG as a negative control. The immunoprecipitated DNA was quantified by real-time PCR using primers specific for the human GAPDH CDS, FOXO3a-promoter, RAB20, and LDHA-promoter regions. The data are presented as enrichment of each sample relative to the total amount of input at each amplicon.

Research Use

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

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References (1)
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