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巨噬细胞炎性蛋白 1 阿尔法定量分析酶联免疫检测试剂盒

本试剂盒仅供科研使用。用于体外定量检测人血清


、血浆或细胞培养上清液中的 CCL3 浓度
。使用前请仔细阅读说明书并检查试剂组分

是否完整

。如有产品包装破损或质量投拆，请在收到货一个月之内联系EBET易博
。

CCL3 简介






：

CCL3



，也叫巨噬细胞炎性蛋白 MIP-1α 属于趋化因子 CC 家族的成员。MIP-1α 的基因与其它 b 族趋化因子家族基因一样，都位于 17 号

染色体上。人的 MIP-1α 的 DNA 编码 92 个氨基酸的前体蛋白

，经过裂解为成熟的 MIP-1α 蛋白和一个 22 个氨基酸的信号肽

。

MIP-1α 一般由活化的 T 细胞、B 细胞

、单核细胞

、肥大细胞、中性粒细胞

、朗格汉斯细胞、星型胶质细胞

、内皮细胞



、成纤维细胞和

平滑肌细胞等产生分泌。

MIP-1α 在免疫调控和炎症反应过程中起重要作用。MIP-1α 能特别对 CD8+ T 细胞以及单核细胞

、巨噬细胞
、树枝状细胞等起化学引诱

和趋化作用
。除了趋化性外，MIP-1α 还具有诱异炎症细胞因子的分泌，肥大细胞的降解以及 NK 细胞的活化等作用。也有报道 MIP-1α 能

够抑制造血干细胞的分化

，有效地维持这类干细胞的去分化状态
。

检测原理:

本试剂盒采用双抗体夹心ELISA法检测样本中CCL3的浓度
。CCL3捕获抗体已预包被于酶标板上


，当加入标本或参考品时



，其中的CCL3

会与捕获抗体结合


，其它游离的成分通过洗涤的过程被除去。当加入生物素化的抗人CCL3抗体后

，抗人CCL3抗体与CCL3接合，形成夹心的

免疫复合物
，其它游离的成分通过洗涤的过程被除去


。随后加入辣根过氧化物酶标记的亲合素

。生物素与亲合素特异性结合
，亲合素连接

的酶就会与夹心的免疫复合物连接起来
；其它游离的成分通过洗涤的过程被除去
。最后加入显色剂

，若样本中存在CCL3将会形成免疫复合

物


，辣根过氧化物酶会催化无色的显色剂氧化成蓝色物质
，在加入终止液后呈黄色
。通过酶标仪检测
，读其450nm处的OD值，CCL3浓度与OD450

值之间呈正比
，通过参考品绘制标准曲线
，对照未知样本中OD值

，即可算出标本中CCL3浓度。

人CCL3定量分析酶联免疫检测试剂盒组成:

组分 规格（96T/48T）

人CCL3预包被板 12条/6条

5×标准品稀释液 10ml/5ml

人CCL3标准品 2支/1支(冻干)

人CCL3生物素化抗体 10ml/5ml

亲和素连接的HRP酶 10ml/5ml

浓缩洗涤液 20× 30ml/15ml

TMB底物 10ml/5ml

中止液 5ml/3ml

封板胶纸 3/2张

说明书 1份

标本收集:

1.标本的收集请按下列流程进行操作；

A.细胞上清标本离心去除悬浮物后即可

；

B.血清标本应是自然凝固后

，取上清




，避免在冰箱中凝固血液


；

C.血浆标本





，推荐用EDTA的方法收集

D.若待测样本不能及时检测，标本收集后请分装
，冻存于－20℃
，避免反复冻融。

2.血清标本不应添加任何防腐剂或抗凝剂
；

3.标本应清澈透明

，检测前样本中如有悬浮物应通过离心去除




。

4.请勿使用溶血

，高血脂或污染的标本检测
，否则结果将不准确


。注意事项:

1.试剂盒请保存在2～8℃
。

2.浓缩洗涤液因在低温下可能有结晶
，请水浴加热使结晶完全溶解后再配制工作液
。

3.标准品复溶加样后


，剩余部份请丢弃。

4.底物请勿接触氧化剂和金属




。

5.加样时
，请及时更换枪头，避免交叉污染
。

6.严禁混用不同批号的试剂盒组份
。

7.充分混匀对保证反应结果的准性很重要
，在加液后请轻轻叩击边缘以保证混匀
。

8.室温反应，请严格控制在25～28℃。

9.洗涤过程是至关重要的
，洗涤不充分会使精确度下降并导致结果误差较大
。

10.试验中标准品和样本检测时建议作双复孔。

11.加样过程中避免气泡的产生

。

12.血清和血浆标本的检测时
，检测抗体的孵育时间应适当延长
。

检测前准备工作:

1.试剂盒自冰箱中取出后应置室温（25-28℃）平衡20分钟
；每次检测后剩余试剂请及时于2～8℃保存


。

2.将浓缩洗涤液用双蒸水或去离子水稀释(1份加19份水)。

3.如有5X准品稀释液，请按所需量用双蒸水或去离子水稀释(1份加4水)

。

4.标准品: 按标签复溶体积加入 1X 标准品稀释液复溶使 CCL3 终浓度达到 500pg/ml


，室温反应，请严格控制在 25～28℃

，静置 15~20 分钟

后轻轻混悬（建议抽吸几次）待彻底溶解


，用标准品稀释液倍比梯度稀释后依次加入检测孔中。（标准曲线取七个点，最高浓度为 500 pg/ml,

标准品稀释液直接加入作为 0 浓度.）

洗涤方法:

自动洗板机或人工洗板

：每孔洗涤液为300ul，注入与吸出间隔15-30秒。洗板5次。最后一次洗板完成后将板倒扣着在厚吸水纸上用力拍干

。

实验过程需自备的材料

：

1.不同规格的加样枪及相应的枪头；

2.酶标仪
；

3.自动洗板机；

4.去离子水或双蒸水；

操作步骤:

1.通过计算并确定一次性实验所需的板条数，取出所需板条放置在框架内，暂时用不到板条请放回铝箔袋密封，保存于4℃。

2.建议设置本底较正孔，即空白孔,设置方法为该孔只加TMB显色液和中止液。每次实验均需做标准品对照并画出标准曲线



。

3.分别将标本或不同浓度标准品(100ul/孔)加入相应孔中，用封板胶纸封住反应孔，室温（25-28℃）孵育120分钟


。对于血清样本的稀释

倍数一般2~15倍稀释，如无准确稀释范围

，从2倍开始稀释。细胞上清需根据实验结果，如果超过试剂盒的检测限


，请相应稀释后再检测
。

4.洗板5次，且最后一次置厚吸水纸上拍干。

5.加入生物素化抗体工作液(100ul/孔)。用封板胶纸封住反应孔
，室温（25-28℃）孵育60分钟



。

6.洗板5次
，且最后一次置厚吸水纸上拍干



。

7.加入亲和素连接的HRP酶工作液(100ul/孔)
。用封板胶纸封住反应孔

，避光室温（25-28℃）孵育20分钟
。

8.洗板5次







，且最后一次置厚吸水纸上拍干。

9.加入显色剂TMB100ul/孔，避光室温（25-28℃）孵育20分钟


。

10.加入中止液50ul/孔,混匀后即刻测量OD450值


。

上海EBET易博生物科技有限公司 www.082786.com人CCL3参考标准曲线

0

0.5

1

1.5

2

2.5

0 15.625 31.25 62.5 125 250 500

人CCL3浓度(pg/ml)

O

D值

上海EBET易博生物科技有限公司 www.082786.com

结果判断:

1.复孔的值在20%的差异范围内结果才有效，复孔的值平均后可作为测量值
。

2.每个标准品或标本的OD值应减去本底校正孔的OD值

。

3.手工绘制标准曲线
。以标准品浓度作横坐标
，OD值作纵坐标
，以平滑线连接各标准品的坐标点
。通过标本的OD值可在标准曲线上查出其

浓度
。

4.若标本 OD 值高于标准曲线上限，应适当稀释后重测
，计算浓度时应乘以稀释倍数

。

典型数值和参考曲线

浓度pg/ml 典型OD值1 典型OD值2 OD平均值

0 0.114 0.098 0.106

15.625 0.253 0.195 0.224

31.25 0.386 0.318 0.352

62.5 0.612 0.494 0.553

125 1.036 0.932 0.984

250 1.623 1.465 1.544

500 2.342 2.166 2.254

人CCL3 参考标准曲线

注意



：本图仅供参考

，应以同次试验标准品所绘标准曲线计算标本含量

。

灵敏度
，特异性和重复性:

1.灵敏度：多次重复结果表明




，最小检出量为4.6pg/ml。

2.特异性：与人的MCP-1、EGF、ENA-78
、G-CSF

、GM-CSF

、IL-1α 
、IL-1β 
、IL-6及小鼠的CCL3无交叉反应性
。

3.重复性
：板内





，板间变异系数均<10%.

参考文献:

1. Kelner, G.S. and A. Zlotnik (1995) J. Leuk. Biol. 57:778.

2. Graham, G.J. et al. (1993) Cell Growth Diff. 4:137.

3. Lukacs, N.W. et al. (1994) Am. J. Pathol. 144:711.

4. Koch, A.E. et al. (1994) J. Clin. Invest. 93:921.

5. Cocchi, F. et al. (1995) Science 270:1811.

6. Schall, T.J. et al. (1993) J. Exp. Med. 177:1821.上海EBET易博生物科技有限公司 www.082786.com

ELISA Kit for the Quantitative Analysis of Human CCL3

The human CCL3 ELISA (enzyme-linked immunosorbent assay) kit is used for detection of human CCL3 in cell culture

supernatants,human serum and plasma.THE ELISA KIT IS FOR RESEARCH USE ONLY. Please read this instruction manual carefully

and check out the material provided before use, and you can contact with our company if any questions. You can enter our website or call

us for other aim.

Introduction

CCL3, also known as MIP-1 alpha (Macrophage Inflammatory Protein 1 alpha), is a member of the CC- subfamily of chemokines.

The gene for MIP-1α has been mapped to chromosome 17, along with all other human b chemokine genes (2). Human MIP-1α cDNA

encodes a 92 aa residue precursor protein with a 22 aa residue signal peptide that is cleaved to generate the secreted mature protein.

MIP-1α has been shown to be produced by activated T cells, B cells, monocytes, mast cells, neutrophils, Langerhans cells,

astrocytes, endothelial cells, fibroblasts and smooth muscle cells (2-7).

MIP-1α play a central role during immunoregulatory and inflammation processes. MIP-1α preferentially attracts CD8+ T cells

and monocytes, macrophages, and dendritic cells..In addition to its chemotactic functions, MIP-1α induces inflammatory cytokine

secretion, mast cell degranulation, and NK cell activation. It has also been reported to inhibit hematopoetic stem cell proliferation and

may be responsible for the maintenance of these cells in a quiescent state.

Principles of the Test

The kits is a solid sandwich enzyme-linked immunosorbent assay for detection of human CCL3. An anti-human CCL3 monoclonal

antibody has been absorbed onto the wells of the microtiter strips provided. Samples including specimens or standards were pipetted into

wells. The human CCL3 in specimens or standards would be captured by the coated antibody and the free others were removed by

washing. The human CCL3 biotin-conjugated antibody were added and binds to human CCL3 captured by the first antibody, which

formed a sandwich. Streptavidin-HRP would be added and binds to the biotin conjugated antibody, then free Streptavidin-HRP would be

removed during a wash step. After this, subtrate solution would be added and catalyzed by the HRP, and a coloured product is formed.

The intensity of the colored product is used to calculate in proportion to the amount of human CCL3 in the original specimen.

Materials provided with the kits:

Reagent 96/48Test Kit

Human CCL3 Antibody-Coated Wells 12 strips/6 strips

5XStandard Diluent 10 ml/5ml

Human CCL3 Standard 2/1vial(s)

Human CCL3 Detetion Antibody 10ml/5ml

Streptavidin-HRP 10ml/5ml

Wash Buffer Concentrate 20× 30ml/15ml

TMB 10ml/5ml

Stop Solution 5ml/3ml

Plate Covers 3/2

Complete Instruction Manual 1

Specimen Collection

1. Collecting specimen as following:

A. The particulate of the cell culture supernatants should be removed before use.

B. Serum was obtained from clot at room temperature.

C. Please collect plasma with EDTA.

D. Assay immediately or store samples at -20℃. Avoid free-thaw cycles.

2. Antiseptic and anticoagulant should not appear in Serum samples.

3. Any particulate should be removed from samples before use.

4. Do not use grossly hemolyzed or lipemic samples.Precautions for use:

1. Please storage the Kit at 2～8℃。

2. Washing buffer concentrate may have crystal in low temperature, and you can melt its in water-bath before use.

3. Please discard the remains after use of the dissolved standard.

4. Avoid contact of substrate solution with oxidizing agents and metal.

5. Usage of disposable pipette tips avoid microbial contamination or cross-contamination of reagents or specimens.

6. Do not mix or substitute reagents with those from other lots or other sources.

7. To ensure the adequate mixure of added reagents, please tap gently the plate after the wells were filled with liquid.

8. Incubation temperature should be 25～28℃.

9. Wash step was crucial for whole assay process.

10. Duplicate wells of the same sample were recommended in assay process.

11. Avoid the foam while pour the liquid into wells.

12. For serum or plasma samples ,the biotin-conjugated antibody should be incubate for at least 90 minutes.

Reagent Preparation

1.The reagents should be warmed up to room temperature before use. The remanent reagents must reseal and put into refrigeratory

again as soon as possible.

2.Dilute 1ml of wash buffer Concentrate into 19ml deionized or distilled water to work.

3. Dilute 1ml of 5×sample diluent into 4ml deionized or distilled water to 1×sample diluent.

4. Add the standard dilution solution to the bottle according to the volume of the label and wait 15 minutes for complete dissolution.

Incubation temperature should be 25～28℃。.And in turn add the half concentration diluent by standard diluent .

Wash step:

Automated microplate washer or operating by pipette: Each well should be pour into300ul wash buffer and soak 15 or 30 seconds,then

be aspirated, five times process were repeated. After the last wash, remove remaining wash buffer by aspirating. Invert the plate and blot

it against clean paper towels.

Materials Required But Not Provided

1. pipettes and pipette tips

2. Microwell strip reader capable of reading at 450 nm (540 nm asoptional reference wave length)

3. automated microplate washer

4.Glass-distilled or deionized water

Assay procedure

1.The needed strips were putted into the frame, the remains were returned into foil pouch and resealed.

2.Blank well were recommended, which only color reagent and stop solution be added. It is suggested that each testing with gradient

density of standard for standard curve.

3.Add 100ul of standard or sample.Cover with the Plate Covers provided.Incubate for 2 hours at room temperature . The suggested

dilution for normal serum/plasma is 2 - 15 fold.If the OD value of sample beyond the Kit scope ,you should re-assay after diluent the

sample.

4.Five times wash process were repeated.

5.Add 100ul of detetion antibody. Cover with the Plate Covers provided.Incubate for 1 hour at room temperature.

6.Five times wash process were repeated.

7.Add 100ul of Streptavidin-HRP. Cover with the Plate Covers provided. Lucifugal incubation for 20 minutes at room temperature.

8.Five times wash process were repeated.

9.Add 100ul of TMB

，Lucifugal incubation for 20 minutes at room temperature.

10.Add 50ul of stop solution to each well, determine the optical

density of each well within 10 minutes

Calculation of Results

1.Duplicates should be within 20 percent of the mean. Average absorbance values for each set of duplicate samples were used as

detection results.

上海EBET易博生物科技有限公司 www.082786.comhuman CCL3 Standard Curve

0

0.5

1

1.5

2

2.5

0 15.625 31.25 62.5 125 250 500

human CCL3 concentration(pg/ml)

O

p

t

i

c

a

l

D

e

n

s

i

t

y

上海EBET易博生物科技有限公司 www.082786.com

2.The blank absorbance values of subtract should be deducted.

3.Drawing a best fit curve through the points of graph. Draw the standard curve by plotting assayed OD valure (on the Y axis) vs.

concentration (on the X axis). The sample concentration was obtained based on its OD value founding in the standard concentration

curve.

4.If the values obtained are not within the expected range of the standard, Samples should be dilute and assay again.

Typical Data and Standard Curve

concentration

(pg/ml)

Typical data 1 Typical data 2 Average

0 0.114 0.098 0.106

15.625 0.253 0.195 0.224

31.25 0.386 0.318 0.352

62.5 0.612 0.494 0.553

125 1.036 0.932 0.984

250 1.623 1.465 1.544

500 2.342 2.166 2.254

Human CCL3 Standard Curve

Sensitivity, Specificity, Repeatability

Sensitivity: repeated assays were evalsuated and the minimum detectable dose was4.6 pg/ml.

Specificity : No significant cross-reactivity or interference with human MCP-1,EGF,ENA-78,G-CSF,GM-CSF,IL-1α ,IL-1β ,IL-6 and

Mouse CCL3.

Repeatability: The coefficient of variation between wells or plates is less than 10 percent.

REFERENCES:

1. Kelner, G.S. and A. Zlotnik (1995) J. Leuk. Biol. 57:778.

2. Graham, G.J. et al. (1993) Cell Growth Diff. 4:137.

3. Lukacs, N.W. et al. (1994) Am. J. Pathol. 144:711.

4. Koch, A.E. et al. (1994) J. Clin. Invest. 93:921.

5. Cocchi, F. et al. (1995) Science 270:1811.

6. Schall, T.J. et al. (1993) J. Exp. Med. 177:1821