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Home >Products> Reagents >Antibody> COX1/Cyclooxygenase 1 Recombinant Rabbit mAb (S-1478-48)
COX1/Cyclooxygenase 1 Recombinant Rabbit mAb (S-1478-48)
COX1/Cyclooxygenase 1 Recombinant Rabbit mAb (S-1478-48)
Origin of place Singapore
Model S0B1175-25μl
Supplier ANT BIO PTE.LTD.
Price 100
Hits 4
Updated 8/27/2025
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Product Specification


HostRabbit
AntigenCOX1/Cyclooxygenase 1
SynonymsProstaglandin G/H synthase 1; Prostaglandin H2 synthase 1 (PGH synthase 1; PGHS-1; PHS 1); Prostaglandin-endoperoxide synthase 1; PTGS1
ImmunogenSynthetic Peptide
LocationEndoplasmic reticulum membrane
AccessionP23219
Clone NumberS-1478-48
Antibody TypeRecombinant mAb
IsotypeIgG
ApplicationWB, IHC-P
ReactivityHu, Ms, Rt
Positive SampleA431, HeLa, HaCaT, C2C12, NIH/3T3, mouse cerebellum, mouse kidney, rat cerebellum, rat kidney
PurificationProtein A
Concentration0.5 mg/ml
ConjugationUnconjugated
Physical AppearanceLiquid
Storage BufferPBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
Stability & Storage

12 months from date of receipt / reconstitution, -20 °C as supplied

Dilution


applicationdilutionspecies
WB1:1000Hu, Ms, Rt
IHC-P1:250Hu, Ms, Rt

Background

COX1, full name Cyclooxygenase-1, is one of the two isoforms of cyclooxygenase (COX), with the other being COX-2. COX1 is a constitutive enzyme that is widely expressed in most tissues such as blood vessels, stomach, kidneys, and platelets. It is involved in platelet aggregation, vascular tone, gastric mucosal blood flow, and regulation of renal blood flow, helping to maintain the stability of cellular, tissue, and organ physiological functions. Compared to COX-2, COX1 is constitutively expressed and plays a role in the synthesis of physiological prostaglandins (PGs), which regulate normal tissue cell activities such as protecting the gastrointestinal mucosa and altering vascular tone. COX1 plays a smaller role in inflammatory damage compared to COX-2. Inflammation primarily stimulates monocytes, macrophages, etc., inducing the production of COX-2, which is a key link in triggering subsequent inflammatory responses.

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