Products for Research Use Only

CTNNB1 Antibody

CAT: 0013-GTR17946414-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17946414-01Size:50 µg
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Description
This CTNNB1 monoclonal Antibody is an unconjugated monoclonal product. It tagets CTNNB1 using a Synthetic Peptide as the immunogen. This antibody is suitable for ELISA, IHC, WB. Purification: The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen..
Product Name Alternative
Anti-CTNNB1 antibody, anti-CTNNB antibody, anti-OK/SW-cl.35 antibody, anti-Catenin beta-1 antibody, anti-Beta-catenin antibody
UniProt
P35222
Reactivity
Human, Mouse, Rat
Immunogen
Synthetic Peptide
Target
CTNNB1
Clonality
Monoclonal
Clone
B9D34
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
Dilution
WB:1:500-1:5000, IHC-P:1:50-1:500
Form
Liquid
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ELISA, IHC, WB
Host or Source
Mouse
Preservative
PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.
Isotype
IgG

UniProtKB · P35222

Catenin beta-1

CTNB1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P35222
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CTNNB1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A8K1L7, Q8NEW9, Q8NI94, Q9H391
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationGlycoproteinPhosphoproteinS-nitrosylationUbl conjugation

Molecular function

Activator

Biological process

Cell adhesionHost-virus interactionNeurogenesisTranscriptionTranscription regulationWnt signaling pathway

Cellular component

Cell junctionCell membraneCell projectionCytoplasmCytoskeletonMembraneNucleusSynapse

Coding sequence diversity

Chromosomal rearrangement

Disease

Disease variantIntellectual disability

Domain

Repeat

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