Products for Research Use Only

ATRX Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18555152Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18555152Size:100 µg
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Description
ATRX Rabbit Polyclonal Antibody (APC)
Product Name Alternative
ATRX chromatin remodeler; JMS; MRX52; RAD54; RAD54L; XH2; XNP; ZNF-HX
UniProt
P46100
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins.
Immunogen
E.coli-derived human ATRX recombinant protein (Position: E8-Q289) .
Target
Transcriptional regulator ATRX
Clonality
Polyclonal
Conjugation
APC
Field of Research
Epigenetics & Chromatin, Immunology & Inflammation, Infectious Disease & Virology, Microbiology, Signal Transduction
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

UniProtKB · P46100

Chromatin remodeler ATRX

ATRX_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P46100
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ATRX
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.6.4.-
Processing
—
Secondary accessions
D3DTE2, P51068, Q15886, Q59FB5, Q59H31, Q5H9A2, Q5JWI4, Q7Z2J1, Q9H0Z1, Q9NTS3
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationIsopeptide bondMethylationPhosphoproteinUbl conjugation

Coding sequence diversity

Alternative splicing

Ligand

ATP-bindingMetal-bindingNucleotide-bindingZinc

Molecular function

Chromatin regulatorDNA-bindingHydrolase

Cellular component

ChromosomeNucleusTelomere

Disease

Disease variantIntellectual disability

Biological process

DNA damageDNA repairTranscriptionTranscription regulation

Domain

Zinc-finger