Home > Product > Antibody > Rabbit Anti-Thromboxane synthase antibody
CYP5; CYP5A1; Cytochrome P450 5A1; TBXAS1; THAS; Thromboxane A synthase 1 platelet cytochrome P450 subfamily V; TS; TXA synthase; TXAS; TXS.
Cat:
SL4019R
Species Reactivity:
Human,Mouse,(predicted: Rat,Dog,Pig,Cow,Horse,)
Immunogen:
KLH conjugated synthetic peptide derived from human Thromboxane synthase:451-533/533
Format:
Liquid
Storage instructions:
Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
WB=1:500-2000ELISA=1:5000-10000not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Product Overview:
Sample: U937(Human) Cell Lysate at 30 ugSpleen (Mouse) Lysate at 40 ugPrimary: Anti-Thromboxane synthase (SL4019R) at 1/1000 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 59 kDObserved band size: 59 kDSample: A549(Human) Cell Lysate at 30 ugPrimary: Anti-Thromboxane synthase (SL4019R) at 1/1000 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 59 kDObserved band size: 59 kD
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Unit:
Price: $
Product PDFs
Datasheet:


Thromboxane Synthase is a useful marker for the detection of native thromboxane synthase in smears, isolated cells, human tissue sections, and for affinity purification of the enzyme. In combination with the markers 27E10, RM 3/1 and 25F9, anti Thromboxane Synthase enables a more precise characterization of inflammatory processes in injured tissues, or in vitro cell-cell interaction studies. Distribution of thromboxane synthase in human tissues: Thromboxane synthase is predominantly produced by macrophages or antigen presenting cells of the myelo-monocytic lineage as shown below. Endothelial cells of placenta and epithelial cells in tonsils and bronchi also express this enzyme.

Subcellular Location:
Endoplasmic reticulum membrane.

Tissue Specificity:
Platelets, lung, kidney, spleen, macrophages and lung fibroblasts.

DISEASE:
Defects in TBXAS1 are the cause of Ghosal hematodiaphyseal dysplasia (GHDD) [MIM:231095]. GHDD is a rare autosomal recessive disorder characterized by increased bone density with predominant diaphyseal involvement and aregenerative corticosteroid-sensitive anemia. Aregenerative anemia is characterized by bone marrow failure, so that functional marrow cells are regenerated slowly or not at all.
Defects in TBXAS1 are the cause of thromboxane synthetase deficiency (TBXAS1 deficiency) [MIM:27436]. It is characterized by hemorrhagic diathesis.

Similarity:
Belongs to the cytochrome P450 family.

SWISS:
P24557

Gene ID:
6916

Database links:

Entrez Gene: 6916 Human

Entrez Gene: 21391 Mouse

Entrez Gene: 397112 Pig

Entrez Gene: 24886 Rat

Omim: 27436 Human

SwissProt: P24557 Human

SwissProt: P36423 Mouse

SwissProt: P47787 Pig

SwissProt: P49430 Rat

Unigene: 520757 Human

Unigene: 4054 Mouse

Unigene: 16283 Rat



Picture

Sample:
U937(Human) Cell Lysate at 30 ug
Spleen (Mouse) Lysate at 40 ug
Primary: Anti-Thromboxane synthase (SL4019R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 59 kD
Observed band size: 59 kD
Sample:
A549(Human) Cell Lysate at 30 ug
Primary: Anti-Thromboxane synthase (SL4019R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 59 kD
Observed band size: 59 kD
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