Protein Concentration Of Mouse Serum

Goat Anti-Mouse IgG-HRP conjugate (adsorbed with human IgG and serum proteins)

40322-200 0.5 ml
EUR 196.8

Human IgG antibody Laboratories manufactures the protein concentration of mouse serum reagents distributed by Genprice. The Protein Concentration Of Mouse Serum reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Mouse Serum. Other Protein products are available in stock. Specificity: Protein Category: Concentration Group: Of Mouse

True Blue

50mg Ask for price
Description: True Blue

True Blue

5mg Ask for price
Description: True Blue

Human IgG rabbit polyclonal antibody, Serum

2 ml Ask for price

Linsmaier and Skoog Vitamin Concentration (Syringe Vials)

100 mL
EUR 43.46

Schenk and Hildebrandt Vitamin Concentration (Syringe Vials)

100 mL
EUR 43.56

McCown and Murashige and Skoog (MS) Vitamin Concentration (Syringe Vials)

100 mL
EUR 42.04

Mouse True insulin ELISA kit

96T
EUR 700
Description: ELISA

Of Mouse information

Cas9 Nickase H840A NLS Protein (High Concentration)

K138 40 µg (250pmol) Volume: 25µL
EUR 135
Description: The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 system is the latest RNA-guided, endonuclease tool in genome editing which allows for very specific genomic disruption and replacement. One concern with the current CRISPR Cas9 technology is the potential off-target effects of the Cas9 nuclease. ;;To improve the off-target mutagenic effects of this system, the Cas9 Nickase H840A Protein was developed with a H840A mutation in its HNH-like nuclease domain. Unlike the Cas9 nuclease, this mutant form generates a single-stranded nick instead of a double-strand break (DSB). Because a single DNA nick is quickly repaired with high fidelity by the cellular machinery, the system requires two closely juxtaposed nicks in order to trigger the same genomic disruption as the Cas9 nuclease. This effectively boosts the recognition sequence to 40 instead of 20 nucleotides, and, as a result, off-target effects become highly unlikely. Thus, the double-nickase CRISPR system offers unparalleled specificity to satisfy even the most stringent of experimental requirements.;;The Cas9 nuclease from the bacteria Streptococcus pyogenes, abbreviated spCas9, is the most commonly used Cas9 variant. The reason for spCas9 popularity is two-fold. First, the spCas9 PAM sequence is 5’-NGG, which is highly abundant in the genome allowing virtually any gene to be targeted. The spCas9 enzyme also has on average a higher efficiency in vivo compared to other variants. Cas9 H840 Nickase NLS contains a SV40 T antigen nuclear localization sequence (NLS) on the C-terminus of the protein.Streptococcus pyogenes, abbreviated spCas9, is the most commonly used Cas9 variant. The reason for spCas9 popularity is two-fold. First, the spCas9 PAM sequence is 5’-NGG, which is highly abundant in the genome allowing virtually any gene to be targeted. The spCas9 enzyme also has on average a higher efficiency in vivo compared to other variants. Cas9 H840 Nickase NLS contains a SV40 T antigen nuclear localization sequence (NLS) on the C-terminus of the protein.

Cas9 Null Mutant GFP NLS Protein (High Concentration)

K186 47µg (250pmol) Volume: 25µL
EUR 155
Description: The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 system is the latest RNA-guided, endonuclease tool in genome editing which allows for very specific genomic disruption and replacement. ;The Cas9 Null Mutant Protein is created by mutating both cleavage domains of the wild type Cas9 (D10A and H840A). Such a Cas9 protein retains its ability to bind to genomic DNA through gRNA:genomic DNA base pairing, however, unlike Cas9 Nuclease and Cas9 Nickase, where permanent gene disruption can be achieved, the Cas9 Null Mutant does not introduce any genome modifications. Therefore, this protein can provide a useful negative control for CRISPR experiments. In addition, binding of the Null Mutant can act as a roadblock to hinder transcription, thus offering a useful tool to achieve reversible knock-down of gene expression. ;The Cas9 from the bacteria Streptococcus pyogenes, abbreviated spCas9, is the most commonly used Cas9 variant. ;The fusion of Cas9 to GFP allows for visual confirmation of transfection as well as subsequent verification of Cas9 clearance from the cells. Cas9 Null Mutant GFP can also be used for FACS applications and screening. Cas9 D10A Null Mutant GFP NLS contains a SV40 T antigen nuclear localization sequence (NLS) on the C-terminus of the protein.

ETHANOL, 70% CONCENTRATION

IB15727 10L
EUR 210.13
Description: BOX W/SPIGOT (HAZ)

ddATP - high concentration

NU-271L 5 x 10µl
EUR 146.8

ddATP - high concentration

NU-271S 10µl
EUR 51.9

ddCTP - high concentration

NU-272L 5 x 10µl
EUR 146.8

ddCTP - high concentration

NU-272S 10µl
EUR 51.9

ddGTP - high concentration

NU-273L 5 x 10µl
EUR 146.8

ddGTP - high concentration

NU-273S 10µl
EUR 51.9

ddTTP - high concentration

NU-274L 5 x 10µl
EUR 146.8

ddTTP - high concentration

NU-274S 10µl
EUR 51.9

Cas9 D10A Nickase GFP NLS Protein (High Concentration)

K149 47µg (250pmol) Volume: 25µL
EUR 155
Description: The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 system is the latest RNA-guided, endonuclease tool in genome editing which allows for very specific genomic disruption and replacement. One concern with the current CRISPR Cas9 technology is the potential off-target effects of the Cas9 nuclease. ;To counteract off-target mutagenic effects of this system, the Cas9 Nickase D10A was developed with a D10A mutation in its RuvC1 nuclease domain. Unlike the Cas9 nuclease, this mutant form generates a single stranded nick instead of a double-strand break (DSB). Because a single DNA nick is quickly repaired with high fidelity by the cellular machinery, the system requires two closely juxtaposed nicks in order to trigger the same genomic disruption as the Cas9 nuclease. This effectively boosts the recognition sequence to 40 instead of 20 nucleotides, and, as a result, off-target effects become highly unlikely. Thus, the double-nickase CRISPR system offers unparalleled specificity to satisfy even the most stringent of experimental requirements. ;The Cas9 from the bacteria Streptococcus pyogenes, abbreviated spCas9, is the most commonly used Cas9 variant. ;The fusion of Cas9 to GFP allows for visual confirmation of transfection as well as subsequent verification of Cas9 clearance from the cells. Cas9 D10A Nickase-GFP can also be used for FACS applications and screening. Cas9 D10A Nickase -GFP NLS contains a SV40 T antigen nuclear localization sequence (NLS) on the C-terminus of the protein.

pSET152- Low concentration

PVT11339 2 ug
EUR 444

pSET152- high concentration

PVT11338 2 ug
EUR 444

Non-Interfering Protein Concentration Determination Kit

SK3071 250Assays, 250preps
EUR 130.99

Lentivirus concentration reagent

E28F06205 100ml
EUR 336.51

MS BASAL SALT CONCENTRATION (20x)

M576 1000ML
EUR 25.31