Proteins

Proteins

Recombinant Proteins

CytoSections

Mass Spec Standards

Mutant Proteins

Native Proteins

Human

CATHEPSIN B

CD10

KALLIKREIN 11

KALLIKREIN 6

CASPASE-7

TMPRSS4

CATHEPSIN L

CPVL

DPP3

DPP6

HAPTOGLOBIN

SENP8

CD71

ECE1

HTRA1

MASP1

MMP1

PEPD

PSMA4

USP8

ARTS1

ASRGL1

ATG4B

ATG4C

CASPASE 1

CASPASE 3

CTSA

EPOXIDE HYDROLASE

HGF

MALT1

MMP3

PGP9.5

PROSTATE SPECIFIC ANTIGEN

PSMB8

SIL1

XPNPEP1

AMINOACYLASE 1

CARBOXYPEPTIDASE A2

CARBOXYPEPTIDASE B

CARBOXYPEPTIDASE H

CATHEPSIN Z

CHYMOTRYPSIN LIKE PROTEASE

CNDP1

COMPLEMENT FACTOR B

CTRB1

IDE

LEGUMAIN

LEUKOTRIENE A4 HYDROLASE

MMP2

OTUB2

PARK7

PLAT

THIMET OLIGOPEPTIDASE

UCHL3

UPA

USP14

XPNPEP3

CAPNS1

MEST

OTUD5

PSMA

USP16

BACE1

CARBOXYPEPTIDASE B2

CARBOXYPEPTIDASE M

CASPASE 9

CD26

FLIP

KALLIKREIN 10

KALLIKREIN 5

L KYNURENINE HYDROLASE

USP1

USP44

ABHD12

ADAMTS8

BACE2

C1S

CALPAIN 9

CATHEPSIN D

CNDP2

CPA4

CPXM

DPP1

DPP8

FACTOR VII

FACTOR X

HPR

KALLIKREIN 1

KALLIKREIN 2

PAN2

PEPSINOGEN II

PGCP

PLASMA KALLIKREIN 1B

PRADC1

PROTHROMBIN

PSMA3

PSMB5

PSMB9

SENP7

TTC35

IHC

HEK293T

HEK293

E. coli

Sf9

Insect

C-Myc/DDK

C-MYC/DDK

C-His

N-His

N-GST and C-His

Myc-DDK

Tag Free

N-GST and C-HIS

C-6xHis

N-GST

N-His&C-His

C-DDK

C-6His

C-Fc

C-HIS

C-HUMAN

N-6His

N-Fc

N-GST, C-His

N-His-PDCD1(Pro21-Val170)

N-His/DDK

Yes

MVPro

SDS PAGE

WB

Druggable Genome

Transmembrane

Transcription Factors

Secreted Protein

Protein Kinase

ES Cell Differentiation/IPS

Protease

Stem cell - Pluripotency

Phosphatase

Ion Channels: Other

Adult stem cells

GPCR

Embryonic stem cells

Nuclear Hormone Receptor

P450

Cancer stem cells

Induced pluripotent stem cells

Stem cell relevant signaling - JAK/STAT signaling pathway

Ion Channels: Potassium

Stem cell relevant signaling - TGFb/BMP signaling pathway

Stem cell relevant signaling - Wnt Signaling pathway

Stem cell relevant signaling - DSL/Notch pathway

Ion Channels: Cys-loop Receptors

ELISA

SDS-PAGE

Ion Channels: Glutamate Receptors

Ion Channels: Transient receptor potential

Ion Channels: ATP Receptors

Bioactivity

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

10 mM Tris-HCl

2 mM dithiothreitol

Ion Channels: Sodium

Enzyme Activity

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. Dulbecco's PBS).

ELISA.
Western Blot.

Flow Cyt

Ion Channels: Cyclic nucleotide gated

pH 7.4). For immunization purposes

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

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

pH 7.4).
For immunization purposes

Ion Channels: Calcium

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

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

e.g. Dulbeccos PBS).

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

pH 7.4).
For immunization purposes

pH 7.4).
For Immunization purposes

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

ELISA.

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoblotting.
Receptor-binding studies.

Western Blot.

0.1% (w/v) insulin

000-1/5

10 mM sodium phosphate

10mM Tris-HCl

1mM DTT

2 mM dithiothreitol

2mM EDTA.
2. Add 4ug of recombinant thioredoxin into reaction cocktail and mix immediately.
3. Incubate at 25°C for 20 minutes.
4. Record the increase in A650nm for 15 minutes

2mM dithiothreitol

63mM sodium phosphate

Biological activity/ Working concentration: The working concentration of ECGF for HUVEC is in the range of 25µg/ml to 100µg/ml. When adding Heparin (2.5mg per mg ECGF) an ECGF concentration of 12µg/ml (30µg/ml Heparin) is optimal. In this case 6mg ECGF are sufficient for 500 ml medium.

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoassays.
Immunization.
Protocol: Reconstitution to filaments: After vimentin is dissolved in 9.5M Urea buffer (see above)

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

Can be used as standard in a Sandwich ELISA.

ELISA.
Western blotting.

FACS

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

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoassays.
Immunization.
Protocol: Reconstitution to filaments: after desmin is dissolved in 9.5 M urea buffer (see above)

Protein standard in 1D and 2D SDS gelelectrophoresis.
Immunoassays.
Immunization.
Protocol: Reconstitution to filaments: after vimentin is dissolved in 6 M urea buffer (see above)

Protocol: 1. Uehara Y.

Protocol: Activity Assay
1. Prepare a 1 ml reaction cocktail into a suitable container: The final concentrations are 5mM Tris

Recombinant E. coli derived Human Sonic HedgeHog is a 20.0 kDa protein consisting of 176 amino acid residues

Suitable for Immunoblotting (Western or Dot blot)

and Fukazawa H. (1991) Methods Enzymol. 201: 370.
2. Fukazawa H.

and Nuccitelli R. (1992) J.Biol.Chem. 267:5608.

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.Dulbecco's PBS).

et al. (1991) Biochem. Pharmacol. 42: 1661.
3. Satoh T.

et al.(1992) J.Biol.Chem. 267: 2537.
4. Weiss R.

including an N-terminal Ile-Val-Ile sequence substituted for the natural occurring chemically modified Cys residue.

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

protofilaments and filament complexes are obtained by dialyzing the resulting polypeptide solution stepwise to a concentration of 4M Urea and then to low salt condition (50mM NaCl

protofilaments and filament complexes are obtained by dialyzing the resulting polypeptide solution stepwise to a concentration of 4M urea and then to low salt condition (50 mM NaCl

the solution can be further dialyzed against PBS (Phosphate Buffered Saline

000) as well as other antibody based fluorescent assays.

000)
Flow Cytometry/FACS (1/1

000-1/200

000-1/32

000-1/40

000.

000.
Immunohistochemistry: 1/1

000.
Protein G Peroxidase is a useful reagent in Western Blotting and ELISA experiments. Protein G Peroxidase can be utilized as a pseudo-secondary detection reagent when used in conjunction with an IgG-based primary antibody and appropriate substrate (such as TMB-1000 or Femtomax-110).

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

000.
Western blot: 1/10

500.
Immunohistochemistry: 1/200-1/1

ELISA.
Western Blot.
Cell culture and/or animal studies.

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.
Western blotting.

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

ELISA.

Functional Assays.

Positive control for Western blot analysis

Positive control for Western blot analysis.
Standard for ELISA.

Adermann K. Role of the prosequence of guanylin. Protein Sci. 1999 Sep; 8(9): 1850-9.
4. Lauber T

Cell culture and/or animal studies.
ELISA.
Western Blot.

Cohen MB. Proguanylin secretion and the role of negative-feedback inhibition in a villous epithelial cell line. Am J Physiol Gastrointest Liver Physiol. 2002 Sep; 283(3): G695-702.
3. Schulz A

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.
Functional Assays.

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.

Forssmann WG

Hawkins JA

Hidaka Y

Immunofluorescence Microscopy (1/1

Immunoperoxidase Electron Microscopy and Immunohistochemistry as well as other peroxidase-biotin-avidin based enzymatic assays.
Recommended Dilutions:
ELISA: 1/20

Marx UC

Marx UC. Native and recombinant proguanylin feature identical biophysical properties and are monomeric in solution. Biochemistry. 2002 Dec 10; 41(49): 14602-12.
2. Rudolph JA

Marx UC. Solution structure of human proguanylin: the role of a hormone prosequence. J Biol Chem. 2003 Jun 27; 278(26): 24118-24. Epub 2003 Apr 21.

Neudecker P

Nourse A

Rosch P

Schulz A

Shimonishi Y

Specific methodologies have not been tested using this product.

Suitable for Immunoblotting (Western or dot blot)

Western Blot.
ELISA.

Western Blot.
Protocol: 1. Lauber T

Western Blotting.

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 (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

Complement and coagulation cascades

Lysosome

Alzheimer's disease

Proteasome

Metabolic pathways

Renin-angiotensin system

Pathways in cancer

Apoptosis

Antigen processing and presentation

Parkinson's disease

Hematopoietic cell lineage

Amyotrophic lateral sclerosis (ALS)

Bladder cancer

Regulation of autophagy

Endocytosis

Huntington's disease

Neuroactive ligand-receptor interaction

Viral myocarditis

p53 signaling pathway

Colorectal cancer

Prostate cancer

Glutathione metabolism

Systemic lupus erythematosus

Alanine

Arachidonic acid metabolism

Focal adhesion

NOD-like receptor signaling pathway

RIG-I-like receptor signaling pathway

aspartate and glutamate metabolism

Arginine and proline metabolism

GnRH signaling pathway

Leukocyte transendothelial migration

Natural killer cell mediated cytotoxicity

Type I diabetes mellitus

Epithelial cell signaling in Helicobacter pylori infection

Wnt signaling pathway

PPAR signaling pathway

Amino sugar and nucleotide sugar metabolism

B cell receptor signaling pathway

Cytokine-cytokine receptor interaction

Cytosolic DNA-sensing pathway

MAPK signaling pathway

Melanoma

Metabolism of xenobiotics by cytochrome P450

Renal cell carcinoma

T cell receptor signaling pathway

Histidine metabolism

beta-Alanine metabolism

Endometrial cancer

Non-small cell lung cancer

Notch signaling pathway

Pancreatic cancer

Protein export

Small cell lung cancer

Tryptophan metabolism

VEGF signaling pathway

Cyanoamino acid metabolism

Regulation of actin cytoskeleton

Selenoamino acid metabolism

Taurine and hypotaurine metabolism

Folate biosynthesis

Glycerolipid metabolism

Neurotrophin signaling pathway

Purine metabolism

Spliceosome

Allograft rejection

Autoimmune thyroid disease

Graft-versus-host disease

Hypertrophic cardiomyopathy (HCM)

Cardiac muscle contraction

Oxidative phosphorylation

Hedgehog signaling pathway

Other glycan degradation

Toll-like receptor signaling pathway

Arrhythmogenic right ventricular cardiomyopathy (ARVC)

Basal transcription factors

Glycosylphosphatidylinositol(GPI)-anchor biosynthesis

Human

Neutrophils

Baculovirus

Human 293

Plasma

1

2

Yes

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