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F11R ELISA Kit

This Colorimetric ELISA kit is designed for the quantitative measurement of Human F11R.
Catalog No. ABIN2859221

Quick Overview for F11R ELISA Kit (ABIN2859221)

Target

See all F11R ELISA Kits
F11R (F11 Receptor (F11R))

Binding Specificity

AA 28-238

Reactivity

  • 5
  • 4
  • 2
  • 1
Human

Detection Method

Colorimetric

Method Type

Sandwich ELISA

Detection Range

46.9-3000 pg/mL

Application

ELISA

Sample Type

Cell Culture Supernatant, Serum
  • Minimum Detection Limit

    46.9 pg/mL

    Purpose

    Sandwich High Sensitivity ELISA kit for Quantitative Detection of Human JAM-A

    Brand

    PicoKine™

    Analytical Method

    Quantitative

    Specificity

    Expression system for standard: E.coli
    Immunogen sequence: S28-V238

    Cross-Reactivity (Details)

    There is no detectable cross-reactivity with other relevant proteins.

    Sensitivity

    <10pg/mL

    Material not included

    Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl

    Immunogen

    Expression system for standard: E.coli
    Immunogen sequence: S28-V238
  • Application Notes

    Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.

    Comment

    Sequence similarities: Belongs to the immunoglobulin superfamily.

    Plate

    Pre-coated

    Protocol

    human JAM-A ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for JAM-A has been precoated onto 96-well plates. Standards(E.coli, S28-V238) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for JAM-A is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the human JAM-A amount of sample captured in plate.

    Assay Procedure

    Aliquot 0.1 mL per well of the 3000pg/mL, 1500pg/mL, 750pg/mL, 375.pg/mL, 187.5pg/mL, 93.8pg/mL, 46.9pg/mL human JAM-A standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of human cell culture supernatants or serum to each empty well. See "Sample Dilution Guideline" above for details. We recommend that each human JAM-A standard solution and each sample is measured in duplicate.

    Assay Precision

    • Sample 1: n=16, Mean(pg/ml): 572, Standard deviation: 22.31, CV(%): 3.9
    • Sample 2: n=16, Mean(pg/ml): 1145, Standard deviation: 49.24, CV(%): 4.3
    • Sample 3: n=16, Mean(pg/ml): 1963, Standard deviation: 102.1, CV(%): 5.2,
    • Sample 1: n=24, Mean(pg/ml): 631, Standard deviation: 35.34, CV(%): 5.6
    • Sample 2: n=24, Mean(pg/ml): 1398, Standard deviation: 85.28, CV(%): 6.1
    • Sample 3: n=24, Mean(pg/ml): 2120, Standard deviation: 156.9, CV(%): 7.4

    Restrictions

    For Research Use only
  • Handling Advice

    Avoid multiple freeze-thaw cycles.

    Storage

    -20 °C,4 °C

    Storage Comment

    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles

    Expiry Date

    12 months
  • Target See all F11R ELISA Kits

    F11R (F11 Receptor (F11R))

    Alternative Name

    F11R

    Background

    Protein Function: Seems to play a role in epithelial tight junction formation. Appears early in primordial forms of cell junctions and recruits PARD3. The association of the PARD6-PARD3 complex may prevent the interaction of PARD3 with JAM1, thereby preventing tight junction assembly (By similarity). Plays a role in regulating monocyte transmigration involved in integrity of epithelial barrier. Involved in platelet activation. In case of orthoreovirus infection, serves as receptor for the virus. .

    Background: Junctional adhesion molecule A(JAM-A) is a protein that in humans is encoded by the F11R gene. It is mapped to 1q23.3. This gene is an immunoglobulin-like molecule that colocalizes with tight junctions in endothelium and epithelium and is also found on blood leukocytes and platelets. JAM-A plays an important role in the regulation of tight junction assembly in epithelia. In addition, it can act as a receptor for reovirus, a ligand for the integrin LFA1, involved in leukocyte transmigration, and a platelet receptor. JAM-A has a nonredundant role in controlling DC motility, trafficking to lymph nodes, and activation of specific immunity.

    Synonyms: Junctional adhesion molecule A,JAM-A,Junctional adhesion molecule 1,JAM-1,Platelet F11 receptor,Platelet adhesion molecule 1,PAM-1,CD321,F11R,JAM1, JCAM,UNQ264/PRO301,

    Full Gene Name: Junctional adhesion molecule A

    Cellular Localisation: Cell junction, tight junction . Cell membrane, Single-pass type I membrane protein . Localized at tight junctions of both epithelial and endothelial cells.

    Gene ID

    50848

    UniProt

    Q9Y624

    Pathways

    Cell-Cell Junction Organization
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