Products for Research Use Only

CCT3 Rabbit Polyclonal Antibody (Cy3)

CAT: 0013-GTR18563303Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18563303Size:100 µg
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Description
CCT3 Rabbit Polyclonal Antibody (Cy3)
Product Name Alternative
T-complex protein 1 subunit gamma; TCP-1-gamma; CCT-gamma; hTRiC5; CCT3; CCTG, TRIC5
UniProt
P49368
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
A synthetic peptide corresponding to a sequence at the C-terminus of human CCT3, different from the related mouse and rat sequences by one amino acid.
Target
T-complex protein 1 subunit gamma
Clonality
Polyclonal
Conjugation
Cy3
Field of Research
Protein Biochemistry, Signal Transduction
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
60534 Da
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 · P49368

T-complex protein 1 subunit gamma

TCPG_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P49368
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CCT3
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
TCP-1-gamma
EC number
3.6.1.-
Processing
—
Secondary accessions
A6NE14, Q5SZY1, Q9BR64
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationDisulfide bondIsopeptide bondPhosphoproteinUbl conjugation

Coding sequence diversity

Alternative splicing

Ligand

ATP-bindingNucleotide-binding

Molecular function

ChaperoneHydrolase

Cellular component

Cytoplasm

Disease

Disease variantIntellectual disability