IA124: NMab Protein L Resin

* Cost competitive, high binging capacity protein L resins.

* High dynamic binding capacity: ~75 mg/mL (Fab, 5 minute residence time).

* Clean in Place: 6 M guanidine hydrochloride.

BP4200: Recombinant Dr. Nuclease

Source: E. coli-derived.
Specific activity: ≥1.1 x 10^6 U/mg. One unit of Dr. Nuclease is defined as the amount of enzyme required to produce a change in absorbance at 260 nm of 1.0 in the time of 30 minutes, under optimum conditions with excess substrate.
Purity: ≥95% by SDS-PAGE and ≥99% by SEC-HPLC. It does not contain any antimicrobial preservatives or protein stabilizers except glycerol (of synthetic origin).

BP4200-GMP: Recombinant Dr. Nuclease, GMP Grade

Source: E. coli-derived.
Predicted molecular mass: ~28 kDa.
Specific activity: ≥1.1 x 10^6 U/mg. One unit of Dr. Nuclease is defined as the amount of enzyme required to produce a change in absorbance at 260 nm of 1.0 in the time of 30 minutes, under optimum conditions with excess substrate.
Purity: ≥95% by SDS-PAGE and ≥99% by SEC-HPLC. It does not contain any antimicrobial preservatives or protein stabilizers except glycerol (of synthetic origin).
Formulation: 0.2 μM filtered solution (250 units/ul) of 20 mM Tris-HCl, pH 8.0, 2 mM MgCl2, 2 mM NaCl, 50% Glycerol.
Endotoxin level: ≤0.01 EU/1000 units following 2020 ChP 1143 USP <85>.
Protease activity: No detectable protease activity using casein as substrate.
Residual host cell protein: ≤10.0 ppm by ELISA.
Mycoplasma: negative by qPCR method.
Bioburden: negative following 2020 ChP 1105 USP <61>.
Residual heavy metal: ≤10.0 ppm following 2020 ChP 0821 USP <32>.

MB127-5G: 5G RT Supermix for qPCR with gDNA Elimination Function

* The 5G RT supermix for qPCR with gDNA elimination function is suitable for two-step RT-qPCR detection, and compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.
* Simple and fast operation: one-step genome clearance and reverse transcription.
* Higher reverse transcription efficiency and higher cDNA yields from all regions of RNA transcripts: based on the more efficient 5G Reverse Transcriptase.
* Flexible choice of primers: Different types of reverse transcription primers can be used flexibly for different experimental designs.
* Excellent cDNA stability: complete deactivation of thermal DNase and long-term storage of cDNA.
 

MB127-4G: 4G RT Supermix for qPCR with gDNA Elimination Function

* The 4G RT supermix for qPCR with gDNA elimination function is suitable for two-step RT-qPCR detection, and compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.
* Based on the highly efficient 4G Reverse Transcriptase, the super temperature tolerance ensures that the complex secondary structure of RNA can be opened under high temperature conditions to obtain longer cDNA.
* Quick and complete removal of genome contamination by the 4 × gDNA Removing Buffer: to ensure more reliable follow-up results, and simplify the design of qPCR primers, without the need to design primers across introns.
* Different primers are selected for different downstream applications.

MB037-5G: 5G First Strand cDNA Synthesis Kit with gDNA Elimination Function

* Higher reverse transcription efficiency and higher cDNA yields from all regions of RNA transcripts: based on the more efficient 5G Reverse Transcriptase.
* Flexible choice of primers: Different types of reverse transcription primers can be used flexibly for different experimental designs.
* Quick and complete removal of genome contamination by the 5× gDNA Removing Buffer: to ensure more reliable follow-up results, and simplify the design of qPCR primers, without the need to design primers across introns.

MB037-4G: 4G First Strand cDNA Synthesis Kit with gDNA Elimination Function

* Based on the highly efficient 4G Reverse Transcriptase, the super temperature tolerance ensures that the complex secondary structure of RNA can be opened under high temperature conditions to obtain longer cDNA.
* A wide range of template starting amount: from 1 pg - 5 μg total RNA.
* Long fragment amplification: up to 15 kb or more.
* Anchored Oligo (dT)23 VN primer is designed for binding site anchoring with high specificity, ensuring the efficiency and success rate of first-strand cDNA synthesis.
* Different primers are selected for different downstream applications. The synthesized one-strand cDNA is widely used in molecular cloning, hybridization, PCR amplification and qPCR reaction, and so on.

IA021: NMab Protein A Resin

* Cost competitive, high binging capacity alkaline-stable protein A resins.

* High dynamic binding capacity: ≥ 55 mg/mL (human IgG, 4 minute residence time).

* Clean in Place: 0.1-0.5 M NaOH.

IA121: NMab Pro Protein A Affinity Resin

* Cost competitive, high binging capacity alkaline-stable protein A affinity resins.

* High dynamic binding capacity: 60 - 80 mg/mL (human IgG, 4 minute residence time).

* Clean in Place: 0.1-0.5 M NaOH.

EK000095-20310: ELISA reagent kit for human Fc protein

The human Fc ELISA Reagent Kit contains the same essential components as human Fc ELISA Complete Kit (EK000095-HUFC).
Application: for the quantitative determination of human Fc proteins in cell culture supernatants and serum.
This assay is specific for human Fc, and does not cross react with mouse Fc.

EK000095-20320: ELISA reagent kit for mouse Fc protein

The mouse Fc ELISA Reagent Kit contains the same essential components as mouse Fc ELISA Complete Kit (EK000095-MOFC).
Application: for the quantitative determination of mouse Fc proteins in cell culture supernatants and serum.
This assay is specific for mouse Fc, and does not cross react with human Fc.

BP002785-ENZ-229: Recombinant Human Seryl-tRNA Synthetase (SARS) Enzyme

Source: E. coli-derived.
Purity: > 90.0% as determined by SDS-PAGE.