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STUB1 Rabbit Polyclonal Antibody

CAT: 0013-GTR18682919-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18682919-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-Human STUB1 Polyclonal Antibodyis a rabbit polyclonal antibody detecting Antigen NY-CO-7 in ELISA, IHC, WB. Suitable for Chicken, Human, Mouse, and Rat. Highlights Affinity Purified: Minimal background and high purity for reliable results. Multi-Application: Validated across multiple applications. Multi-Species: Cross-reactive for translational research.
Product Name Alternative
Antigen NY-CO-7, CHIP, CLL-associated antigen KW-8, STUB1, Carboxy terminus of Hsp70-interacting protein, STIP1 homology and U box-containing protein 1, E3 ubiquitin-protein ligase CHIP, RING-type E3 ubiquitin transferase CHIP
UniProt
Q9UNE7
Reactivity
Gallus, Human, Mouse, Rat
Immunogen
E. coli - derived recombinant Human STUB1 (Ser23-Tyr303) .
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Epigenetics & Chromatin
Purification
Purified by antigen affinity column.
Concentration
Lot dependent
Form
Liquid
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.
Tested Applications
ELISA, IHC, WB
Host or Source
Rabbit
Preservative
0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.
Isotype
IgG

UniProtKB · Q9UNE7

E3 ubiquitin-protein ligase CHIP

CHIP_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9UNE7
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
STUB1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.3.2.27
Processing
—
Secondary accessions
A2IDB9, O60526, Q969U2, Q9HBT1
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

CytoplasmMitochondrionNucleus

Disease

Disease variantNeurodegenerationSpinocerebellar ataxia

Biological process

DNA damageDNA repairUbl conjugation pathway

PTM

Isopeptide bondPhosphoproteinUbl conjugation

Domain

RepeatTPR repeat

Molecular function

Transferase

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