SETD5 Rabbit pAb (APR20693N)

CAT: 0882-APR20693N-01Size: 50 µLDry Ice: NoHazardous: No

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CAT#:0882-APR20693N-01Size:50 µL

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24/48H Stock Items & 2 to 6 Weeks non Stock Items.

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Background

This function of this gene has yet to be determined but mutations in this gene have been associated with autosomal dominant mental retardation-23. Alternative splicing results in multiple transcript variants encoding different isoforms.

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 SETD5 Rabbit pAb (APR20693N) .

Synonyms

SETD5

Gene ID

55209

UniProt

Q9C0A6

Dilution

IHC 1:50 - 1:200 IF 1:50 - 1:200

Form

Liquid

Buffer

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Molecular Weight

Calculated MW: 145kDa/147kDa/157kDa

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=55209

Uniprot URL

https://www.uniprot.org/uniprot/Q9C0A6

AA Sequence

HAFENLEKRKKRRDQPLEQSNSDVEITTTTSETPVGEETKTEAPESEVSNSVSNVTIPSTPQSVGVNTRRSSQAGDIAAEKLVPKPPPAKPSRPRPKSRISRYRTSSAQRLKRQKQANAQQAELSQAALEEGGSNSLVTPTEAGSLDSSGENRPLTGSDPTVVSITGSHVNRAASKYPKTKKYLVTEWLNDKAEKQECPVECPLRITTDPTVLATTLNMLP

UniProtKB · Q9C0A6

Histone-lysine N-methyltransferase SETD5

SETD5_HUMAN · Homo sapiens

View on UniProt ↗

Primary accession: Q9C0A6
Review status: UniProtKB reviewed (Swiss-Prot)
Gene: SETD5
Protein existence: 1: Evidence at protein level
Organism: Homo sapiens (Human)
Taxonomy ID: 9606
Alternative names: —
EC number: 2.1.1.359, 2.1.1.367
Processing: —
Secondary accessions: Q6AI17, Q8WUB6, Q9H3X4, Q9H6V7, Q9H7S3, Q9NVI9

Protein keywords

Coding sequence diversity

Alternative splicing

Disease

AutismAutism spectrum disorderDisease variantIntellectual disability

Molecular function

Chromatin regulatorMethyltransferaseTransferase

Cellular component

ChromosomeNucleus

PTM

Phosphoprotein

Technical term

Proteomics identificationReference proteome

Biological process

TranscriptionTranscription regulation

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