Products for Research Use Only

PPP2R5C Antibody

CAT: 0013-GTR18140870Size: 400 μlDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0013-GTR18140870Size:400 μl
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
PPP2R5C Antibody
Product Name Alternative
Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform, PP2A B subunit isoform B'-gamma, PP2A B subunit isoform B56-gamma, PP2A B subunit isoform PR61-gamma, PP2A B subunit isoform R5-gamma, Renal carcinoma antigen NY-REN-29, PPP2R5C, KIAA0044
UniProt
Q13362
Reactivity
Human
Immunogen
This PPP2R5C antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 465-494 amino acids from the C-terminal region of human PPP2R5C.
Target
PPP2R5C
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Signal Transduction
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Concentration
Batch dependent
Form
Liquid
Molecular Weight
61 kDa
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
For WB starting dilution is: 1:1000
Tested Applications
WB
NCBI Accession Number
Q13362
Host or Source
Rabbit
Preservative
Supplied in PBS with 0.09% (W/V) sodium azide.
Isotype
Rabbit Ig

UniProtKB · Q13362

Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform

2A5G_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q13362
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
PPP2R5C
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
B4DYJ8, B5BUA5, F5GWP3, Q14391, Q15060, Q15174, Q6ZN33
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Coding sequence diversity

Alternative splicing

Cellular component

CentromereChromosomeNucleus

Disease

Disease variantIntellectual disability