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BAP1 Antibody

CAT: 0013-GTR18194604-02Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18194604-02Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Mouse monoclonal antibody to BAP1
Product Name Alternative
Anti-BAP1 antibody, anti-BRCA1 associated protein 1 antibody, anti-Cerebral protein 13 antibody, anti-Cerebral protein 6 antibody, anti-HUCEP 13 antibody, anti-Hucep 6 antibody, anti-HUCEP13 antibody, anti-Hucep6 antibody, anti-TPDS antibody, anti-Ubiquitin carboxy terminal hydrolase antibody, anti-Ubiquitin carboxyl terminal hydrolase BAP1 antibody, anti-UCHL2 antibody
UniProt
Q92560
Reactivity
Human
Immunogen
Recombinant human BAP1 protein fragment (around aa 191-326) (exact sequence is proprietary)
Target
BAP1
Clonality
Monoclonal
Clone
BAP1/2665
Conjugation
Unconjugated
Field of Research
Epigenetics & Chromatin
Purification
Protein A/G
Concentration
200 μg/ml
Form
200ug/ml of Ab Purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with 0.05% rAlbumin & 0.05% azide. Also available WITHOUT rAlbumin & azide at 1.0mg/ml.
Molecular Weight
91kDa
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
Host or Source
Mouse
Isotype
IgG

UniProtKB · Q92560

Ubiquitin carboxyl-terminal hydrolase BAP1

BAP1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q92560
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
BAP1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.4.19.12
Processing
—
Secondary accessions
A8K993, Q6LEM0, Q7Z5E8
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Molecular function

Chromatin regulatorDevelopmental proteinHydrolaseProteaseThiol protease

Cellular component

ChromosomeCytoplasmNucleus

Domain

Coiled coil

Biological process

DifferentiationUbl conjugation pathway

Disease

Disease variantIntellectual disability

PTM

PhosphoproteinUbl conjugation

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