beta2-GP1 Ab IgA ELISA 试剂盒
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- 抗原 See all beta2-GP1 Ab IgA products
- beta2-GP1 Ab IgA (Beta2-Glycoprotein 1 Antibody IgA (beta2-GP1 Ab IgA))
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适用
- 人
- 检测方法
- Colorimetric
- 实验类型
- Competition ELISA
- 应用范围
- ELISA
- 原理
- ß2GP1 IgA Enzyme-linked Immunosorbent Assay (ELISA) is intended for the detection and semiquantitative determination of IgA antibodies to ß2GP1 in human sera or plasma.
- Analytical Method
- Semi-Quantitative
- 特异性
- 98 %
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Beta2-Glycoprotein 1 Antibody IgA (beta2-GP1 Ab IgA) ELISA Kit
beta2-GP1 Ab IgA 适用: 人 Colorimetric Sandwich ELISA 0.313 ng/mL - 20 ng/mL Plasma, Serum, Tissue Homogenate
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- 说明
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Quality Control:
The negative control and positive control should be run with every batch of samples tested and the concentration must be within the range stated on its label. The O.D. value of calibrator 0 SAU must be lower than 0.150 and the O.D. value of calibrator 160 SAU must be greater than 0.750. Additional controls may be prepared from human serum specimens and kept under -20 °C.
Limitations of procedure:
1. Diagnosis cannot be made on the basis of anti beta2 GP1 results alone. These results must be used in conjunction with information from clinical evaluation and other diagnostic procedure.
2. The clinical significance of beta2 GP1 antibodies in diseases other than SLE is currently under investigation.
3. When negative anti beta2 GP1 titers are found in the presence of clinical indications, a lupus anticoagulant, anti-cardiolipin or other additional testing is indicated.
4. It is to be expected that some samples can be anti-cardiolipin positive yet anti beta2 GP1 negative. The anti beta2 GP1 test is a more specific marker of thrombotic risk. The anticardiolipin test can produce false positive results due to cross-reactivity with dsDNA or certain infectious disease antibodies. - 样本量
- 5 μL
- 实验时间
- 1 - 2 h
- 板类型
- Pre-coated
- 试剂准备
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- Prepare 1x washing buffer. Prepare washing buffer by adding distilled or deionized water to 20x wash concentrate to make a final volume of 1 L.
2. Bring all specimens and kit reagents to room temperature (20- 25 °C) and gently mix.
- Prepare 1x washing buffer. Prepare washing buffer by adding distilled or deionized water to 20x wash concentrate to make a final volume of 1 L.
- 样品制备
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- Collect blood specimens and separate the serum.
2. Specimens may be refrigerated at 2-8 °C for up to seven days or frozen for up to six months. Avoid repetitive freezing and thawing of serum sample.
- Collect blood specimens and separate the serum.
- 实验流程
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- Place the desired number of coated strips into the holder.
Moderate positive: 40 - 70 SAU PRE-WASH Coated Wells - Repeat washing three times with washing buffer.
High positive: > 70 SAU Prepare 1:101 dilution of test samples by adding 5 μL of the sample to 500 μL of Sample Diluent. Mix well. Do not dilute 1:101 prediluted Calibrators & Controls. A positive result suggests the possibility of certain autoimmune disease thrombolic disorders. A negative result indicates no beta2 GP1 IgA antibody or levels below the detection limit of the assay. Dispense 100 μL of diluted sera and prediluted calibrators & controls into the appropriate wells. Tap the holder to remove air bubbles from the liquid and mix well. Incubate for 30 minutes at room temperature. Remove liquid from all wells. Repeat washing three times with washing buffer. Dispense 100 μL of enzyme conjugate to each well and incubate for 30 minutes at room temperature. Remove enzyme conjugate from all wells. Repeat washing three times with washing buffer. Dispense 100 μL of TMB Chromogenic Substrate into each well and incubate for 15 minutes at room temperature. Add 100 μL of Stop solution to stop reaction.
- Place the desired number of coated strips into the holder.
- 结果分析
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- Construct a standard curve by plotting O.D. 450 nm on the y-axis against the concentration of calibrator APL values on the x-axis on a log-log graph paper or log-lin graph.
2. Using the O.D. value of each specimen, determine the concentration from the standard curve.
3. A typical example:
Each laboratory is recommended to establish it own normal range based upon its own techniques, controls, equipments and patient population according to their own established procedures. The followings are a suggestive guideline. Negative: < 20 SAU Low positive: 20 - 40 SAU INTERFERENCE AND CROSS-REACTIVITY 3 4 5 6 7 8 9 10.
- Construct a standard curve by plotting O.D. 450 nm on the y-axis against the concentration of calibrator APL values on the x-axis on a log-log graph paper or log-lin graph.
- 实验精密度
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Intra-assay in Mean SAU SD % CV Serum A 8 14.9 0.35 2.38 Serum B 8 30.8 1.39 4.52 Serum C 8 58.9 0.99 1.68 2
Inter-assay in Mean SAU SD % CV Serum A 8 15.6 0.38 2.4 Serum B 8 31.2 1.42 4.55 Serum C 8 59.3 1.05 1.77 - 限制
- 仅限研究用
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- 储存条件
- 4 °C
- 有效期
- 12 months
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- 抗原 See all beta2-GP1 Ab IgA products
- beta2-GP1 Ab IgA (Beta2-Glycoprotein 1 Antibody IgA (beta2-GP1 Ab IgA))
- Abstract
- beta2-GP1 Ab IgA 产品
- 物质类
- Antibody
- 背景
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Cardiolipin autoantibodies (ACA) are described for various autoimmune diseases. The presence of anti-cardiolipin antibodies in systemic lupus erythematosus (SLE) can be related to the development of thrombocytopenia, in gynaecology they are supposed to cause intrauterine death or recurrent abortion. Furthermore, anti-cardiolipin antibodies have been found in some non-thrombotic neurological disorders like cerebrovascular insufficiency, cerebral ischemia or chorea and in myocardial infarction.
Recent studies have shown that a 50kD serum cofactor is required for anticardiolipin antibodies, to bind to cardiolipin which has been coated onto plastic plates. The cofactor has been identified as beta 2 -glycoprotein 1 also termed apolipoprotein H. beta 2 GP1 has been known as an in vitro inhibitor of the intrinsic blood coagulation pathway, ADP-dependent aggregation, and prothrombinase activity of activated platelets. It has become apparent that anticardiolipin antibody from patients with anti-phospholipid syndrome (APS) recognize a modified beta 2 GP1 structure and not cardiolipin, native beta 2 GP1 or an epitope structurally defined by both cardiolipin and beta 2 GP1.
Galli et al. and Viard, et al. reported that anti-cardiolipin antibody derived from SLE and APS were directed to the beta 2 GP1 molecule coated on polystyrene plates. Koike and Matsuura showed conclusively that beta 2 GP1 is indeed the antigen to which many anticardiolipin antibody patients are actually binding and furthermore showed that the phospholipid merely serves to link the beta 2 GP1 to the solid phase. beta 2 GP1 autoantibodies are found in the immunoglobulin classes IgG, IgM and IgA. The determination of IgM antibodies is a valuable indicator in the diagnosis of beginning autoimmune disease, whereas IgG and/or IgA antibodies will be found in progressive stages of manifested autoimmune disorders. IgA antibodies are often associated with IgG antibodies. The determination of IgA antibodies seems to have a greater validity in thrombosis and fetal loss. Indications for determination of anti beta 2 GP1 antibodies are: SLE, Thrombosis, Thrombocytopenia, Cerebral Ischemia, Chorea, Epilepsy, Recurrent Abortion and Intrauterine Death.
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