Products for Research Use Only

PGP9.5 (7B8G5E7) Mouse mAb

CAT: 0013-GTR18243066-01Size: 20 ulDry Ice: NoHazardous: No
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CAT#:0013-GTR18243066-01Size:20 ul
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
PGP9.5 (7B8G5E7) Mouse mAb
Product Name Alternative
UCHL1 / PGP9.5; UCHL1; B220; CD 45; CD45; cd45 antigen; ec3.1.3.48; GP 180; GP180; Human homolog of severe combined immunodeficiency due to PTPRC deficiency; L CA; L-CA; lca; Leukocyte common antigen; LY 5; LY5; Protein tyrosine phosphatase receptor type C; Protein tyrosine phosphatase receptor type c polypeptide; PTPRC; PTPRC_HUMAN; Receptor-type tyrosine-protein phosphatase C; SCID due to PTPRC deficiency; t200; T200 glycoprotein; T200 leukocyte common antigen.
UniProt
P09936
Reactivity
Human
Immunogen
Purified recombinant human UCHL1 / PGP9.5 protein fragments expressed in E.coli.
Target
UCHL1
Clonality
Monoclonal
Clone
B9D0XI7XG9
Conjugation
Unconjugated
Field of Research
Cell Biology
Purification
Affinity Purified
Concentration
2.21 mg/ml
Dilution
WB: 1/500-1/1000 IF: 1/50-1/200
Form
Liquid
Molecular Weight
Calculated MW: 25 kDa; Observed MW: 25 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.
Tested Applications
ICC, IF, WB
Preservative
Liquid in PBS containing 50% glycerol, 0.5% rAlbumin and 0.02% sodium azide, pH 7.3.
Isotype
IgG2b

UniProtKB · P09936

Ubiquitin carboxyl-terminal hydrolase isozyme L1

UCHL1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P09936
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
UCHL1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
UCH-L1
EC number
3.4.19.12
Processing
Precursor
Secondary accessions
Q4W5K6, Q71UM0
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationGlycoproteinLipoproteinOxidationPhosphoproteinPrenylation

Coding sequence diversity

Alternative initiation

Cellular component

CytoplasmEndoplasmic reticulumMembrane

Disease

Disease variantHereditary spastic paraplegiaNeurodegenerationParkinson diseaseParkinsonism

Molecular function

HydrolaseProteaseThiol protease

Biological process

Ubl conjugation pathway