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SET1A Rabbit pAb (APR24327N)

CAT: 0882-APR24327N-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0882-APR24327N-01Size:50 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
The protein encoded by this gene is a component of a histone methyltransferase (HMT) complex that produces mono-, di-, and trimethylated histone H3 at Lys4. Trimethylation of histone H3 at lysine 4 (H3K4me3) is a chromatin modification known to generally mark the transcription start sites of active genes. The protein contains SET domains, a RNA recognition motif domain and is a member of the class V-like SAM-binding methyltransferase superfamily.
Overview
We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality SET1A Rabbit pAb (APR24327N) .
Synonyms
Set1; KMT2F; Set1A; SETD1A; SET1A
Gene ID
9739
UniProt
O15047
Dilution
WB 1:500 - 1:2000
Form
Liquid
Buffer
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Molecular Weight
Calculated MW: 186kDa Observed MW: 300kDa
Storage Conditions
Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Gene ID URL
https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=9739
Uniprot URL
https://www.uniprot.org/uniprot/O15047
AA Sequence
Email for sequence

UniProtKB · O15047

Histone-lysine N-methyltransferase SETD1A

SET1A_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O15047
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
SETD1A
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.1.1.364
Processing
—
Secondary accessions
A0A804HLA6, A6NP62, Q6PIF3, Q8TAJ6
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Molecular function

ActivatorChromatin regulatorMethyltransferaseRNA-bindingTransferase

Cellular component

ChromosomeCytoplasmNucleus

Disease

Disease variantEpilepsyIntellectual disability

Biological process

DNA damageTranscriptionTranscription regulation

PTM

Phosphoprotein

Ligand

S-adenosyl-L-methionine