PA001340-C10882: CSTF1 Polyclonal Antibody
Rabbit Polyclonal Antibody;
Applications: WB, ELISA;
Reactivity: Human, Mouse, Rat.PA003923-PA1911: DLL1 Polyclonal Antibody
Rabbit Polyclonal Antibody;
Applications: WB;
Reactivity: Human, Rat, Mouse.
Isotype: Rabbit IgG.C022: Eculizumab Biosimilar Stable Cell Line (CHO)
The Eculizumab biosimilar stable cell line alone can be transferred alone or together with the technology of process development and/or antibody purification.
C022P: Eculizumab Biosimilar, Human C5 Monoclonal Antibody
Recombinant Humanized IgG2/4 Monoclonal Antibody.
Specificity/Sensitivity: The monoclonal antibody Eculizumab biosimilar specifically binds to the human C5, the terminal complement component 5.
Applications: ELISA, functional assays such as bioanalytical PK and ADA assays.BP001968-PRO-1059: Recombinant Human Exosome Component 5 (EXOSC5) Protein
Source: E. coli-derived.
Purity: > 90% as determined by SDS-PAGE.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.PA000069-R12-2271: NOS1 Polyclonal Antibody
Rabbit Polyclonal Antibody;
Applications: WB, ELISA;
Reactivity: Human.PA000069-MA1072: Nitric Oxide Synthase, Brain (1-181) NOS1 Monoclonal Antibody
Mouse Monoclonal Antibody;
Applications: WB;
Reactivity: Human, Rat;
Clone: N1;
Isotype: Mouse IgG1.PA000069-PA1329: NOS1 Polyclonal Antibody
Rabbit Polyclonal Antibody;
Applications: WB, IHC-P;
Reactivity: Human, Mouse, Rat;
Isotype: Rabbit IgG.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.