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KMT2D Antibody

CAT: 0864-A74065-50ULSize: 50 μLDry Ice: NoHazardous: No
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CAT#:0864-A74065-50ULSize:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
AAD10, ALL1 related gene, ALL1-related protein, ALR, CAGL114, Histone-lysine N-methyltransferase MLL2, KABUK1, Kabuki make up syndrome, Kabuki mental retardation syndrome, KMS, KMT2B, KMT2D, Lysine N methyltransferase 2D, Lysine N-methyltransferase 2B, MLL2, MLL2_HUMAN, MLL4, Myeloid/lymphoid or mixed lineage leukemia 2, Myeloid/lymphoid or mixed-lineage leukemia protein 2, TNRC21, Trinucleotide repeat containing 21
UniProt
O14686
Host
Rabbit
Antigen Species
Human
Reactivity
Human
Target Antigen
Synthetic peptide of Human KMT2D
Target
KMT2D
Clonality
Polyclonal
Conjugation
Non-conjugated
Field of Research
Epigenetics and Nuclear Signaling
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.05% sodium azide, 40% glycerol, pH 7.4.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · O14686

Histone-lysine N-methyltransferase 2D

KMT2D_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O14686
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
KMT2D
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
Lysine N-methyltransferase 2D
EC number
2.1.1.364
Processing
—
Secondary accessions
O14687
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationIsopeptide bondMethylationPhosphoproteinUbl conjugation

Coding sequence diversity

Alternative splicing

Molecular function

Chromatin regulatorMethyltransferaseTransferase

Domain

Coiled coilRepeatZinc-finger

Disease

Congenital hypothyroidismDeafnessDisease variantIntellectual disability

Ligand

Metal-bindingS-adenosyl-L-methionineZinc

Cellular component

Nucleus

Biological process

TranscriptionTranscription regulation

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