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CD141 rabbit pAb

CAT: 0855-ES7386-02Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0855-ES7386-02Size:100 µL
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Background
The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia. [provided by RefSeq, Jul 2008]
Description
The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia. [provided by RefSeq, Jul 2008],
Product Name Alternative
THBD; THRM; Thrombomodulin; TM; Fetomodulin; CD antigen CD141
UniProt
P07204
Swiss Prot
P07204
Reactivity
Human; Rat; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human THBD. AA range:526-575
Target
CD141
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.
Buffer
-20°C/1 year
Molecular Weight
60kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
60kD
Fragment
IgG
Subcellular Location
Membrane; Single-pass type I membrane protein.
Other Product Names
THBD; THRM; Thrombomodulin; TM; Fetomodulin; CD antigen CD141
Gene ID (Human)
7056

UniProtKB · P07204

Thrombomodulin

TRBM_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P07204
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
THBD
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
TM
EC number
—
Processing
Precursor
Secondary accessions
Q8IV29, Q9UC32
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Biological process

Blood coagulationHemostasis

Disease

Disease variantHemolytic uremic syndromeThrombophilia

PTM

Disulfide bondGlycoproteinHydroxylationProteoglycan

Domain

EGF-like domainRepeatSignalTransmembraneTransmembrane helix

Cellular component

Membrane

Molecular function

Receptor