HumanAlkalinePhosphatasestainingoftransgenicembryo/tissue

AP Buffer:100 mM Tris-HCl, pH 9.5100 mM NaCl10 mM MgCl2PTM:PBS0.1% Tween-202 mM MgCl2Since this is generally done in conjunction with lacZ staining, embryo/tissue is usually fixed as per lacZ staining. For wholemount staining, penetration of stain may be improved by fixing in PBS + 0.2% glutaraldehyde + 0.02% NP-40 + 0.01% NaDC (at 4oC).Rinse in PBS.Heat inactivate endogenous alkaline phosphatase activity by incubati......阅读全文

Human-Alkaline-Phosphatase-staining-of-transgenic-embryo/tissue

AP Buffer:100 mM Tris-HCl, pH 9.5100 mM NaCl10 mM MgCl2PTM:PBS0.1% Tween-202 mM MgCl2Since this is generally done in conjunction with lacZ staining, e

Alkaline-phosphatase-staining

4.5.1.1 General informationEndothelial cells possess an endogenous alkaline phosphatase (AP) activity. The enzymatic activity of AP is not restricted

Human-Placental-Alkaline-Phosphatase-Stain

The following protocol is for detection of human placental alkaline phosphatase (AP) in cultured cells. Human placental AP is heat stable, unlike othe

ALKALINE-PHOSPHATASE-(APAAP)-TECHNIQUE

Preparation: Cytological PreparationsFixation: Air dry films or cytospin preparations overnight at room temperature. For frozen and paraffin sections

Phosphatasing-with-Shrimp-Alkaline-Phosphatase-(S.A.P.)

Phosphatasing with Shrimp Alkaline Phosphatase (S.A.P.)Use to prevent linearized vector plasmid from recircularizing.The phosphatase from shrimp is ea

转基因

DNA PreparationGene TransferEmbryo TransferTransgenic IdentificatioinOthersTransgenic Outline (University of Michigan Transgenic Animal Model Core)Thi

Staining-Procedure-for-Flow-Cytometric-Detection-of-Human-Cyclins

Staining Procedure for Flow Cytometric Detection of Human CyclinsThis is a standard protocol used at Pharmingen for Quality Control testing of the ant

骨碱性磷酸酶(bone-alkaline-phosphatase)临床意义

正常参考范围:女:10~22U/L男:12~33U/L临床意义:1反映成骨细胞的活性或骨形成情况,成骨细胞活性和骨形成增加,骨碱性磷酸酶活性增加。2升高可见于patet`s病、原发性甲状旁腺机能亢进、骨软化和肾性营养不良等。

碱性磷酸酶(alkaline-phosphatase,-ALP)的分离与纯化

一、实验目的1.掌握酶分离纯化的一般步骤及相关原理;2.悉碱性磷酸酶的分离纯化的方法步骤。二、实验原理有机溶剂分级沉淀是分离蛋白质的常用方法之一。有机溶剂能使许多溶于水的酌生物大分子发生沉淀,其主要作用是降低水溶液的介电常数。例如20℃时水的介电常数为80,82%的乙醇溶液的介电常数为40。溶液的介

组织学——包埋技术

Tissue Preparation for Methy Methacrylate EmbeddingMethyl Methacrylate Embedding Protocols (Energy Beam Sciences, Inc.)General protocol for plastic em

Histochemical-staining-of-sea-urchin-embryos-for-(AP)-enzyme-activity

Histochemical staining of sea urchin embryos for alkaline phosphatase (AP) enzyme activity1. Obtain embryo samples, tube of AP substrate buffer and tu

Immunohistochemistry

实验概要The following  procedure describes the application of peroxidase or alkaline  phosphatase conjugates in the immunohistochemical labeling of  forma

3-Color-Staining:-AlphaCatenin-in-HeLa-Human-Cervical-Cancer-Cells

实验概要Alpha-catenin  in HeLa human cervical cancer cells was labeled using mouse  anti-α-catenin and visualized with Alexa Fluor® 488 goat anti-mouse Ig

Western-杂交

Western 杂交(主要内容如下)Preparing of Protein LysatesWestern BlottingFar Western BlottingSemi Dry BlottingStripping MembranesTrouble Shooting and OthersPrepa

组织学——染色

Hematoxylin and Eosin Staining of Tissue for LCM (Arcturus)   Immunohistochemical Staining (IHC) (Arcturus)For optimal LCM from IHC samples, it is nec

细菌检测

Gram Staining (+\-) (William H. Heidcamp)  Gram-Staining Procedure (MEDIC, U of Texas)Very nice and detailed method description for Gram staining  Aci

免疫组织化学

·         Double Peroxidase (HRP) Immunohistochemical Labeling of Trypsin-Sensitive Antigens (KPL)·         Immunohistochemistry (Tyner lab)This is a

Dephosphorylation-...

实验概要The method  provides a protocol for removal of phosphate groups from proteins,  before or after blotting. To demonstrate the specificity of an ant

使用CCCadvanced™FN1无异源耗材培养人多能干细胞(三)

Figure 2: hiPSCs proliferation during long-term expansionA. Cumulative cell population doublings for hiPSCs cultured on the FN1 motifs surface as we

Look-Ma,-No-Archenteron!-Sulfates-role-in-sea-urchin-early-development

ObjectiveTo observe the role sulfate plays in sea urchin gastrulation, and to replicate the findings of Karp and Solursh, that sea urchin embryos fail

Genotyping-Transgenic-Rodents-by-PCR

Genotyping Transgenic Rodents by PCRThis is how we test mice and rats for the presence of the transgene by PCR. It is provided for those investigators

DNA的酶学操作

DNA的酶学操作DNA Modifying Enzymes (Michael Blaber)Introduction to bacterial restriction/modification system. It provides very useful background knowledge

寡核苷酸的相关操作

In this section, you will find techniques related to oligonucleotides, such as oligo purification by acrylamide gel, annealing two oligos to make doub

Alkaline-agarose-gel-electrophoresis

Alkaline agarose gel electrophoresis (Sambrook et al., 1989)Alkaline agarose gels can be used to determine the size and quality of first and second st

Fluorescent-Staining-of-Cells

1. Fluorescent phalloidin in methanol. Phallacidin does not work as well. Dilute 10 ul 330 nM stock into 500 ul PBS for each large coverslip.2. PB

Staining-Methods-for-cell

death Z. Xia 10/2/95The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidiu

Wholemount-staining-of-embryos

Fix embryos in formalin or MEMFA for one hour at room temperature with mixing. Rinse with TBS, replace with methanol, store at -20oC.Rehydrate by slow

Intracellular-Staining-Protocol

1. Fix cells- Add16% formaldehyde directly into culture medium to obtain a final concentration of 1.5% formaldehyde.2. Incubate in fixative for 10 min

Silver-Staining-Protocol

1x 40min - overnight     50% MeOH, 12% Acetic Acid1x 30min                                  50% MeOH, 12% Acetic Acid, 0.05% 37% Formaldehyde3x 20min 

Protein-Staining-Procedures

This method was successful in our lab using prostate tissue and for our specific objectives. Investigators must be aware that they will need to tailor