AssayGenie重组人CD164/Endolyn蛋白(His标签)(RPES3015)

Sialomucin 核心蛋白 24 也称为 endolyn 或 CD164(分化簇 164)是一种由人 CD80+ 造血祖细胞表达的新型 90 至 34-kD 粘蛋白样分子。CD1的亚型3和亚型164在造血和非造血组织中表达。亚型1由前列腺癌肿瘤和前列腺癌细胞系表达。骨转移的表达大于原发性肿瘤。骨转移的表达大于软组织转移。CD2的亚型164在小肠,结肠,肺,甲状腺以及结直肠和胰腺腺癌中表达。亚型4由造血祖细胞和骨髓基质细胞表达。CD164属于CD164家族。分化簇(指定簇)(通常缩写为CD)是一种用于鉴定和研究最初存在于白细胞上的细胞表面分子的方案,但在几乎任何类型的身体细胞中发现,为细胞的免疫表型提供靶标。CD164可能在前列腺癌转移和癌细胞浸润骨髓中起重要作用。CD164通过增强CXCR4依赖性......阅读全文

Pectinase-assay

Pectinases are actually a mixture of enzymes, which, along with others such as cellulase, are widely used in the fruit juice industry where they are

Protease-assay

In certain fruits, such as pineapples and mangoes, the flesh contains protein-digesting enzymes (proteases). These may play a part in helping to soft

Protease-assay

实验概要         In certain fruits, such as pineapples and mangoes, the flesh contains protein-digesting enzymes (proteases). These may play a part

DGK-Assay

Buffers: - 2X buffer 10 ml 0.5 M imidazol, pH 6.6 0.21 g LiCl 1.25 ml 1 M MgCl2 1.0 ml 0.1 M EGTA, pH 6.6 --> Bring volume up to 50 ml with distille

Phosphate-Assay

1. Make standards using sodium phosphate at the following uM concentrations: 0, 2, 5, 7, 10, 20, 40, 60, and 80. Use the screw top glass tubes.2. Dry

Polygalacturonase-assay

This enzyme is famous for being involved in the development of the GMO tomatoes (more information from the link at the foot of this page). The cells o

Aspartate-Assay

实验概要The  Aspartate Assay Kit provides a simple, convenient assay to measure  aspartate in a variety of samples. In the assay, aspartate is converted  

Bradford-Assay

The bradford dye-binding assay is a colorimetric assay for measuring total protein concentration. It involves the binding of Coomassie Brilliant blue

MTT-Assay

 This procedure is for cells in 96 well plates, if larger plates are used then adjust volumes accordingly.1 Make a solution of 5mg/ml MTT dissolved in

Bradford-Assay

Bradford AssayThe bradford dye-binding assay is a colorimetric assay for measuring total protein concentration. It involves the binding of Coomassie B

Chemotaxis-Assay

PurposeThe purpose of a chemotaxis assay is to determine whether your protein or small molecule of interest has chemotactic activity on a specific cel

TUNEL-assay

PROTOCOL:•Deparaffinize and rehydrate slides:3 x 3´ Xylene3 x 2´ 100% ethanol1 x 2´ 95%, 80%, 70% ethanol (each)1 x 5´ 1x PBS•Microwave antigen retrie

Motility-Assay

DescriptionVarious phenotypic characteristics are requiredfor a cancer cell to successfully complete the metastaticcascade. Among these, acquisition o

Assay-of-Phospholipase-A-Activity

Phospholipases of the A type constitute a large family of esterases that catalyze the hydrolysis of the fatty acid ester bonds in phospholipids a

Actin-Capture-Assay

David Amberg Dialyze purified GST fusion proteins and actin into PBS + 1mM MgCl2 . Mix 5ug actin into 50ul total volume binding buffer. Mix

Needle-Assay-for-Chemotaxis

Devreotes Lab, John Hopkins Medical Institutions http://www.hopkinsmedicine.org/cellbio/devreotes/needle.htm Equipment and chemicals Zeiss

Assay-for-the-Micrococcal-Nuclease

Method: Essentially that described by Heins et al. (1966) based upon the release of acid soluble oligonucleotides following nuclease digestion of DNA

BIURET-PROTEIN-ASSAY

BIURET PROTEIN ASSAY MATERIALS Biuret Reagent Bovine serum albumin (BSA) Spectrophotometer and tubes PROCEDURE Prepare standard d

In-vitro-Sphingomyelinase-Assay

Reagents: Lysis buffer 25 mM Tris-HCl, pH 7.4 5 mM EDTA 1 mM ATP 20 µg/ml CLAP 1 mM PMSF Buffer A 10 mM MgCl2 0.2 M Tris-HCl, pH 7.4 0.2 % Triton X

ELISA-Inhibition-Assay

ELISA Inhibition AssaySensitize a 96-well microtiter plate with purified antigen.Prepare a solution of the purified antigen of interest in phosphate b

cell-proliferation-assay

cell proliferation assaybefore start:thaw cells from liquid nitrogen, grow in 75cc flask (T75) in Fischer's medium MM (maintenance medium) until c

HISTONE-KINASE-ASSAY

PROTOCOLTo 1.5 mL eppendorf tubes add:200 µg of protein extract (see Western blot protocol for protein sample preps)q.s. to 300 µL with RIPA (with pro

Bradford-protein-assay

Bradford protein assayConsiderations for useThe Bradford assay is very fast and uses about the same amount of protein as the Lowry assay. It is fairly

Glycolipid-Binding-Assay

Glycolipid Binding AssaySource: Contributed by Pingsunjim, Paller’s LabAbstract: This protocol can be used for the detection of glycolipids binding to

DNA-methyltransferase-Assay

Methylated CpG island Amplification Protocol written by Minoru Toyota2. Materials2.1. MCARestriction enzymes SmaI, XmaIT4 DNA ligaseTaq DNA polymerase

Protein-Assay-(Spectrophotometer)

Protein Assay (Spectrophotometer)Use BSA (bovine serum albumin) 1mg/ml stock solution (1ml Eppendorf tubes) for standard curve.Place 0, 2, 5, 10, 15,

Noble-Agar-Assay

DescriptionCancer cells do not show anchorage and contact inhibition of growth. To assess the anchorage and contact independent growth of cells, noble

LOWRY-PROTEIN-ASSAY

The Lowry procedure is one of the most venerable and widely-used protein assays, being first described in 1951 [Lowry et al., J. Biol. Chem. 193: 265-

Crystal-Violet-Assay

This is a simple assay useful for obtaining quantitative information about the relative density of cells adhering to multi-well cluster dishes. The dy

Migration-Assay-Protocol

Materials to be prepared beforehand:1) FBS free medium2) 10% FBS medium3) Cell migration filter insert ( Transwell®, 12mm Diameter, 12 μm Pore Size.)P