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CTNNB1 Antibody (N-term)

CAT: 0013-GTR18325940-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18325940-01Size:50 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Affinity Purified Rabbit Polyclonal Antibody (Pab)
Product Name Alternative
Catenin beta-1, Beta-catenin, CTNNB1, CTNNB
UniProt
P35222
Reactivity
Human
Immunogen
This CTNNB1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 78-106 amino acids from the N-terminal region of human CTNNB1. Antigen Region: 78-106 aa.
Target
CTNNB1 (HGNC:2514)
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Dilution
IF - 1:50, WB - 1:2000, IHC-P - 1:50, FC - 1:50
Form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Molecular Weight
85497 Da
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.
Prediction Reactivity
Mouse, Other, Rat, Zebrafish
Tested Applications
FC, IF, IHC-P, WB
NCBI Accession Number
NP_001091680.1, NP_001091679.1, NP_001895.1
Host or Source
Rabbit
Isotype
Rabbit 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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