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Anti-PROS1 / Protein S Antibody LS-C38606

Ordering

Wt. Vol. Conc. Price
500 µg - - $545
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
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Most Popular PROS1 / Protein S Antibodies

Anti-PROS1 / Protein S Antibody (clone PS7) LS-C140068
Rat Monoclonal [clone PS7] (IgG2a) to Human PROS1 / Protein S
Human
Western blot, Flow Cytometry
Unconjugated
Anti-PROS1 / Protein S Antibody (clone PS7, FITC) LS-C140069
Rat Monoclonal [clone PS7] (IgG2a) to Human PROS1 / Protein S
Human
Western blot, Flow Cytometry
FITC Conjugated
Anti-PROS1 / Protein S Antibody (aa251-300) IHC-plus™ LS-B6903
Rabbit Polyclonal to Human PROS1 / Protein S
Human, Monkey, Mouse, Rat, Bat, Bovine, Dog, Horse
IHC - Paraffin, Western blot
Unconjugated
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Sheep Polyclonal (IgG) to Human PROS1 / Protein S
Human
ELISA, Immunoelectrophoresis
Unconjugated

Details

Human PROS1 / Protein S
Sheep
Human (tested or 100% immunogen sequence identity)
IgG Polyclonal
Unconjugated
Immunoaffinity purified
Unmodified

Applications

  • ELISA
  • Immunoelectrophoresis

Specificity and Use

PROS1 / Protein S antibody was raised against human Protein S (PS) purified from plasma.
Specific for human Protein S.
Suitable for use in Immunoelectrophoresis and ELISA for Protein S. ELISA: capture.

Packaging

0.01 M HEPES, pH 7.4, 0.15 M sodium chloride, 50% glycerol. No preservatives added.
For research use only.

About PROS1 / Protein S

P07225 NM_000313 NP_000304.2

PROS1 Antibody, Protein S (alpha) Antibody, Protein S alpha Antibody, Protein Sa Antibody, PS22 Antibody, PS21 Antibody, Vitamin K-dependent protein S Antibody, THPH5 Antibody, THPH6 Antibody, PROS Antibody, PS24 Antibody, Protein S Antibody, PS23 Antibody, PS25 Antibody

PROS1 / Protein S is a vitamin K-dependent plasma protein that functions as a cofactor for the anticoagulant protease, activated protein C (APC) to inhibit blood coagulation. It is found in plasma in both a free, functionally active form and also in an inactive form complexed with C4b-binding protein. Mutations in this gene result in autosomal dominant hereditary thrombophilia. An inactive pseudogene of this locus is located at an adjacent region on chromosome 3.

Requested From: United States
Date Requested: 12/3/2016

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