Human Anti-Bovine Amnion Type V Collagen IgG Antibody Assay Kit, TMB

Human Anti-Bovine Amnion Type V Collagen IgG Antibody Assay Kit, TMB - Cat Number: 2082T From Chondrex.

Research Field: Arthritis, Immunology

Clonality: N/A

Cross-Reactivity:

Host Origin: N/A

Applications: N/A

Isotype: N/A

Detection Range: 16 units/ml-0.25 units/ml

Sample Type: Serum, Plasma

Concentration: N/A

Immunogen:

PRODUCT SPECIFICATIONS

DESCRIPTION: Assay kit to quantify human/monkey anti-collagen antibodies
FORMAT: Pre-coated 96-well ELISA Plate with removeable strips
ASSAY TYPE: Indirect ELISA
ASSAY TIME: 4.5 hours
STANDARD RANGE: 16 units/ml to 0.25 units/ml
NUMBER OF SAMPLES: Up to 38 (duplicate) samples/standard plate (will vary for custom kits)
SAMPLE TYPES: Serum and Plasma
RECOMMENDED SAMPLE DILUTIONS: 1:100 (at least)
CHROMOGEN: OPD (read at 490 nm)
STORAGE: -20°C
VALIDATION DATA: N/A
NOTES: This kit has an overnight incubation step

INTRODUCTION

Human serum, especially from patients with autoimmune diseases, contain high levels of immunoreactive components, which yield high background levels in ELISA systems. These non-specific reactions are caused by adhesive immunoglobulins in human serum which so strongly adhere to plastic surfaces by hydrophilic binding that blocking agents such as bovine serum albumin (BSA) and Tween 20 are not capable of blocking these non-specific reactions at all. False positive reactions caused by the serum samples themselves are usually overlooked and are considered real antibody-antigen reactions in many cases, even now. In order to obtain the real values of antigenantibody reactions, it is critical 1) to choose proper blocking agents which block these kinds of non-specific reactions effectively, 2) to determine the unique non-specific background value of each individual sample using antigen-non-coated wells, and 3) to subtract that background value from the corresponding value determined in antigen-coated wells. In addition, it is important to determine the non-specific reactions caused by the secondary antibody as well. Chondrex, Inc.’s ELISA system incorporates unique blocking agents that inhibit the hydrophobic binding of these serum components onto plastic surfaces and are designed to determine the background values of individual samples using antigen-non-coated wells.

Human serum, especially from patients with autoimmune diseases, contain high levels of immunoreactive components, which yield high background levels in ELISA systems. These non-specific reactions are caused by adhesive immunoglobulins in human serum which so strongly adhere to plastic surfaces by hydrophilic binding that blocking agents such as bovine serum albumin (BSA) and Tween 20 are not capable of blocking these non-specific reactions at all. False positive reactions caused by the serum samples themselves are usually overlooked and are considered real antibody-antigen reactions in many cases, even now. In order to obtain the real values of antigenantibody reactions, it is critical 1) to choose proper blocking agents which block these kinds of non-specific reactions effectively, 2) to determine the unique non-specific background value of each individual sample using antigen-non-coated wells, and 3) to subtract that background value from the corresponding value determined in antigen-coated wells. In addition, it is important to determine the non-specific reactions caused by the secondary antibody as well. Chondrex, Inc.’s ELISA system incorporates unique blocking agents that inhibit the hydrophobic binding of these serum components onto plastic surfaces and are designed to determine the background values of individual samples using antigen-non-coated wells.

KIT COMPONENTS

PLATE COATING AND SETUP

Standard ELISA Kit with One Species of Type I or Type II Collagen

A standard ELISA kit consisting of five 8-well strips which are uncoated and serve as a control for background levels of
individual samples, five 8-well strips coated with one species of type V collagen to determine specific antibody levels, and two 8-
well strips for reference standards. “B” represents blank wells to determine non-specific reactions caused by the secondary
antibody. Standards and samples are run in duplicate.

ASSAY OUTLINE

NOTES BEFORE USING ASSAY
NOTE 1: It is recommended that the standard and samples be run in duplicate.
NOTE 2: Warm up all buffers to room temperature before use.
NOTE 3: Crystals may form in Wash Buffer, 20X when stored at cold temperatures. If crystals have formed, warm the wash buffer by placing
the bottle in warm water until crystals are completely dissolved.
NOTE 4: Measure exact volume of buffers using a serological pipet, as extra buffer is provided.
NOTE 5: Cover the plate with plastic wrap or a plate sealer after each step to prevent evaporation from the outside wells of the plate.
NOTE 6: For partial reagent use, please see the assay protocol’s corresponding step for the appropriate dilution ratio. For example, if the
protocol dilutes 50 µl of a stock solution in 10 ml of buffer for 12 strips, then for 6 strips, dilute 25 µl of the stock solution in 5 ml of buffer.
Partially used stock reagents may be kept in their original vials and stored at -20⁰C for use in a future assay.
NOTE 7: This kit contains animal components from non-infectious animals and should be treated as potential biohazards in use and for
disposal.