Products for Research Use Only

PRUNE1 Rabbit Polyclonal Antibody (Cy3)

CAT: 0013-GTR18536836Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18536836Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-PRUNE1 Antibody. Tested in ELISA, IF, ICC, WB, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat.
Product Name Alternative
DRES 17; DRES17; hPrune; HTCD37; Protein prune homolog; PRUNE
UniProt
Q86TP1
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins.
Immunogen
E.coli-derived human PRUNE1 recombinant protein (Position: M1-Q444) .
Target
Exopolyphosphatase PRUNE1
Clonality
Polyclonal
Conjugation
Cy3
Field of Research
Immunology & Inflammation, Neuroscience
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
14377 Da
Storage Conditions
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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 · Q86TP1

Exopolyphosphatase PRUNE1

PRUN1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q86TP1
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
PRUNE1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.6.1.14, 3.6.1.25
Processing
—
Secondary accessions
B2RCH8, B4DFL7, Q5SZF9, Q659E5, Q6P4E0, Q8N654, Q96JU5, Q9C071, Q9C072, Q9UIV0
Protein keywords

PTM

AcetylationPhosphoprotein

Coding sequence diversity

Alternative splicing

Cellular component

Cell junctionCytoplasmNucleus

Disease

Disease variantIntellectual disabilityNeurodegenerationPrimary microcephaly

Molecular function

Hydrolase

Ligand

ManganeseMetal-binding

Technical term

Proteomics identificationReference proteome