Products

Proteins

Expression Plasmids

Primary Antibodies

shRNA Plasmids

siRNA Oligo Duplexes

Knockout Kits (CRISPR)

Recombinant Proteins

qPCR Primer Pairs

Over-expression Lysates

CRISPRa Kits

qPCR Template Standards

CytoSections

3' UTR Clones

Mass Spec Standards

Mutant ORF Clones

MicroRNA Expression Plasmids

ELISA Kits

Secondary Antibodies

IHC Kits and Reagents

Tag Antibodies

TissueScan

Isotype Controls

Organelle Marker Plasmids

qPCR Primer Panels

Mutant Proteins

Mammalian Expression Vectors

CRISPR Vectors

DNA Sequencing Primers

First Strand cDNA

Native Proteins

Lentiviral Gene Expression Vectors

Others

AAV Control Particles

qPCR Reagents

Lentiviral Particles

Assay Reagents

Transfection Reagents

shRNA Vectors

Conjugation Kits

IHC Control Slides (Phase II)

cDNA Clone Sets

Forensic DNA

Luciferase Assay Kits

Cloning Accessories

Bacterial Expression Vectors

CRISPR Accessories

Lenti Titer Kits

AAV Gene Expression Vectors

Antibody Purification Reagents

Lentiviral Packaging Kits

Stable Cell Lines

cDNA Synthesis Kits

Molecular Tools

Reporter Vectors

Virus Antibodies

Lenti Concentrators

Lenti Stabilizers

Mutant CytoSections

3' UTR Assay Vector

Cell Line Lysates

Kinase Collections

MicroRNA Vector

Mycoplasma

TissueScan Starter Kits

Human

Bovine

Chicken

Mouse

AHSG

DES

GFAP

KRT18

KRT8

RNA5-8SN2

APOB

AVD

CEACAM5

COL1A1

COL4A1

COL6A1

CST3

CTSG

ELANE

FSHB

GC

MPO

NEFH

NEFM

PLG

PRSS1

SERPINC1

TTR

Glucose Oxidase

Druggable Genome

10 mM Tris-HCl

2 mM dithiothreitol

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoassays.
Immunization.

Secreted Protein

the solution can be further dialyzed against PBS (phosphate buffered saline

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoassays.
Immunization.
Protocol: Reconstitution to filaments is performed by mixing equimolar amounts of keratins of type I and type II at concentrations of approx. 0.5 mg/ml

both dissolved in 9.5 M urea buffer (see above). Protofilaments and filament complexes are obtained by dialyzing the resulting polypeptide solution stepwise to a concentration of 4 M urea and then to low salt condition (50 mM NaCl

e.g. Dulbeccos PBS).
See References 2 and 3 for more details.

pH 7.4).
For Immunization purposes

Protease

Biological activity/ Working concentration: Optimum concentration for human umbilical vein endothelial cells (HUVEC) range from 50-200 μg/ml

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoassays.
Immunization.
Protocol: Reconstitution to Filaments is performed by dissolving in 6 M urea buffer (see above) at concentrations of approx. 0.5 mg/ml. Protofilaments and filament complexes are obtained by dialyzing the resulting polypeptide solution stepwise to a concentration of 4 M urea and then to low salt condition (50 mM NaCl

Protein standard in 1D and 2D SDS gel electrophoresis.
Immunoassay.
Antigen for immunization.

Suitable for Immunoblotting (Western or Dot blot)

Transmembrane

e.g. Dulbeccos PBS).

pH 7.4).
For immunization purposes

000-1/32

000.

000.
Western Blot: 1/500-1/2

500.
Immunohistochemistry: 1/200-1/1

ELISA.
Suitable for use as a Control or standard in indirect trapping ELISA for quantitation of antigen in serum using a standard curve.
Immunoprecipitation.
Western blotting.

ELISA.
Western Blot.

ELISA: this protein is suitable for use as a Mouse IgE standard in ELISA assays.

ELISA.

ELISA and Immunohistochemistry as well as other beta galactosidase-avidin/biotin based enzymatic assays. This product has been assayed against 1.0 µg of biotinylated IgG in a standard capture ELISA using OPNG as a substrate for 30 minutes at room temperature.
Recommended Dilutions:
ELISA: 1/8000-1/32000.
Western Blot: 1/500-1/2500.
Immunohistochemistry: 1/200-1/1000.

ELISA and immunohistochemistry as well as other glucose oxidase-antibody based enzymatic assays.
Recommended Dilutions:
ELISA: 1/8

ELISA.

ELISA.
Western Blot.

ES Cell Differentiation/IPS

For use as a Control or Standard in Indirect trapping ELISA for quantitation of antigen in serum using a standard curve

For use as a Control or standard in indirect trapping ELISA for quantitation of antigen in serum using a standard curve.
Immunoprecipitation.
Western blotting.

Specific methodologies have not been tested using this product.

change growth medium against basal medium (EBM) in the early afternoon]
- change EGF against EBM (for HUVEC: EBM +1-2% FCS)
- incubate 24 h
- change medium again and add factors (growth factors

etc.)
- incubate for 18 h
- add 10 µl 3H-Thymidine solution [0.025 mCi/ml] per well (=0.25 µCi)
- incubate another 6h at 37°C
- Washing steps: (250 µl/well)
PBS 1x
MeOH 2x 5 min
TCA 2x 10 min
H2O 1x
- lyse cells in 250 µl 0.3M NaOH per well
- transfer 2.5 ml ECO Plus into the appropriate scintillation vials
- transfer cell lysats into the scintillation vials
- count by liquid scintillation (ß-counter; Beckmann Instruments)

for immunoprecipitation and for Wwestern blotting.

inhibitors

optimal concentration with heparin (30 μg/ml) is about 12 μg/ml.

optimal concentration with heparin (50 μg/ml) is about 12 μg/ml.
Protocol: Thymidine Incorporation with HUVEC
- plate cells with a density at 5-7 x 10e3 cells/well in growth medium (EGM)
- incubate cells over night [if urgent

plate cells in the morning

Neuroactive ligand-receptor interaction

ECM-receptor interaction

Focal adhesion

Amyotrophic lateral sclerosis (ALS)

Complement and coagulation cascades

Pathogenic Escherichia coli infection

Systemic lupus erythematosus

GnRH signaling pathway

Lysosome

Pathways in cancer

Renin-angiotensin system

Small cell lung cancer

Plasma

Spinal Cord

Brain

Liver

Placenta

Erythrocytes

Gizzard

Neutrophils

Stomach

Carcinoma

Cell culture

Egg white

Leukocytes

Pancreas

Pituitary

S. avidinii

Serum

Urine

2

3

Yes