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Human IP-10 Standard
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BD™ Cytometric Bead Array (CBA) Human IP-10 Standard

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This product contains lyophilized recombinant human interferon-γ-induced protein-10 (IP-10). When reconstituted, this product can be used as a standard control with the BD™ CBA Human IP-10 Flex Set (Cat. No. 558280). Please refer to the technical data sheet included with the BD™ CBA Human IP-10 Flex Set for further information.

BD™ Cytometric Bead Array (CBA)
Human (QC Testing)
Flow cytometry (Routinely Tested)


Store the lyophilized standard at 4°C prior to reconstitution.

Lyosphere(s) from 1 vial of Human IP-10 Standard, when reconstituted in 4.0 mL Assay Diluent, approximates the CBA activity of Human IP-10 at a concentration of 2500 pg/mL. Following reconstitution, maintain the Human IP-10 at 4°C and use within 12 hours. Any unused reconstituted standard must be discarded after this period (do not store or reuse).


The Human IP-10 Standard has been tested to assure to function as a standard when used with the BD™ Cytometric Bead Array (CBA), such as the BD™ CBA Human IP-10 Flex Set (Cat. No. 558280).  Investigators are encouraged to refer to the technical data sheet for the BD™ CBA Human IP-10 Flex Set (Cat. No. 558280).  An abbreviated instruction has been provided below (Preparation of Human IP-10 Standard Protocol).  The Human IP-10 Standard should be reconstituted using Assay Diluent, which is provided with the BD™ CBA Human Soluble Protein Master Buffer Kit (Cat. No. 558264 or 558265) or it may also be purchased separately (Cat. No. 560104).

Preparation of Human IP-10 Standard:  The Human IP-10 Standard is lyophilized and should be reconstituted and serially diluted before mixing with CBA capture beads and PE detection reagents.

1.  Open one vial of the lyophilized Human IP-10 Standard. Transfer the lyosphere(s) to a polypropylene tube (BD Falcon™, Cat. No. 352097). Label the tube "Top Standard".

2.  Reconstitute the standard with 4.0 mL of Assay Diluent. Allow the reconstituted standard to equilibrate for at least 15 minutes before making dilutions. Mix the reconstituted protein by pipette only. Do not vortex or mix vigorously.

3.  Label additional 12 x 75 mm tubes (BD Falcon™, Cat. No. 352008) and arrange them in the following order: Top Standard, 1:2, 1:4, 1:8, 1:16, 1:32, 1:64, 1:128, and 1:256.

4.  Add 500 µl of Assay Diluent to each of the dilution tubes.

5.  Perform a serial dilution by transferring 500 µl from the Top Standard to the 1:2 dilution tube and mix thoroughly. Do not vortex, mix by pipet only. Continue making serial dilutions by transferring 500 µl from the 1:2 tube to the 1:4 tube and so on to the 1:256 tube and mix thoroughly. Prepare one tube containing only Assay Diluent to serve as the 0 pg/mL negative control.


  1. ProClin is a trademark of Rohm and Haas Company.
  2. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
  3. Please refer to for technical protocols.
  4. Warning: CBA lyophilized standard contains 0.02% (w/w) and Detection Reagent (Part A) contains 0.002% (w/w) of a CMIT/MIT mixture (3:1), which is a mixture of: 5-chloro-2-methyl-4-isothiazolin-3-one [EC No 247-500-7] and 2-methyl-4-isothiazolin-3-one [EC No 220-239-6] (3:1).Hazard statement: May cause an allergic skin reaction.Precautionary statements: Contaminated work clothing should not be allowed out of the workplace. Wear protective gloves/eye/face protection. Wear protective clothing. Avoid breathing mist/vapours/spray. If skin irritation or rash occurs: Get medical advice/attention. IF ON SKIN: Wash with plenty of water. Take off contaminated clothing and wash it before reuse. Dispose of contents/container in accordance with local/regional/national/international regulations.
558466 Rev. 7

Please refer to Support Documents for Quality Certificates

Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described

Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.