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Beta Catenin Rabbit Polyclonal Antibody

CAT: 0013-GTR18308180Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18308180Size:100 µL
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Description
Beta Catenin Rabbit Polyclonal Antibody
Product Name Alternative
Catenin beta 1 , CTNNB , EVR7 , MRD19 , armadillo
UniProt
P35222
Reactivity
Human, Mouse
Immunogen
Recombinant protein encompassing a sequence within the center region of human beta Catenin. The exact sequence is proprietary.
Target
Catenin beta 1
Clonality
Polyclonal
Conjugation
Unconjugated
Purification
Purified by antigen-affinity chromatography.
Concentration
1.01 mg/ml (Please refer to the vial label for the specific concentration.)
Dilution
WB: 1:500-1:3000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
Form
Liquid
Molecular Weight
85
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.
Applications Notes
Positive control: A549 , Mouse brain , HeLa
Tested Applications
ICC, IHC, IHC-P, WB
Host or Source
Rabbit
Preservative
0.1M Tris, 0.1M Glycine, 10% Glycerol, 0.01% Thimerosal.
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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