Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
Catalogue Number
Ordering Description
Qty/Pack
List
この品目はお気に入りに追加されました。
動物種
パネルタイプ
選択したキット
数量
カタログ番号
注文内容
Qty/Pk
価格
96-Well Plate
数量
カタログ番号
注文内容
Qty/Pk
価格
その他の試薬を追加 （MAPmatesとともに使用するにはバッファーおよび検出キットが必要です）
数量
カタログ番号
注文内容
Qty/Pk
価格
48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
Space Saver Option（チェックを入れると箱詰めから袋詰めに変更となりますのでご注意ください） Customers purchasing multiple kits may choose to save storage space by eliminating the kit packaging and receiving their multiplex assay components in plastic bags for more compact storage.
o-Phenylenediamine, 1.0 mg/ml in citrate buffer, pH 4.5, 0.1% urea hydrogen peroxide at 25°C was used as a substrate for testing conjugate enzyme reactivity. Variables associated with assay conditions will dictate the proper working dilution.
Biological Information
Purity
Single band 50,000 on SDS-PAGE
Concentration Label
Please refer to vial label for lot-specific concentration
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code
Blue Ice Only
Toxicity
Standard Handling
Storage
+2°C to +8°C
Do not freeze
Yes
Mercury prohibited
To comply with ban of sale of mercury-added products required by The Interstate Mercury Education and Reduction Clearinghouse (IMERC), this product is prohibited to be sold in the following US states: Rhode Island and Connecticut.
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
13-August-2007 RFH
Application
Direct Immunoassay (1:10,000)
Description
Native protein A from Staphylococcus aureus conjugated to horseradish peroxidase.
Background
Protein A is the universal secondary antibody because it binds to the Fc portions of most immunoglobulin classes. It is a versatile and economic means to isolate, detect and purify antibodies produced by many animals. It is especially useful in immunohistochemical studies because, unlike secondary antibodies, it does not bind to cell Fc receptors and therefore will not give high background reactions.
Form
Liquid
Formulation
In 10 mM PBS, 0.5 mM EDTA, 10% mannose, 2% sucrose, 1% BSA, pH 7.6.
Concentration Label
Please refer to vial label for lot-specific concentration
Purity
Single band 50,000 on SDS-PAGE
Preservative
0.02% thimerosal
Comments
o-Phenylenediamine, 1.0 mg/ml in citrate buffer, pH 4.5, 0.1% urea hydrogen peroxide at 25°C was used as a substrate for testing conjugate enzyme reactivity. Variables associated with assay conditions will dictate the proper working dilution.
