
Outcomes of patients with CLL sequentially resistant to both BCL2 and BTK inhibition
Covalent Bruton tyrosine kinase inhibitors (BTKis) and the BCL2 inhibitor venetoclax have significantly improved outcomes for patients with chronic lymphocytic leukemia (CLL), especially those with biologically adverse disease. Patients with CLL resistant to their first targeted agent (TA) can be effectively treated with the alternative class. However, relapses are expected with second-line TA therapy, and the clinical challenge of double class-resistant disease is now emerging with increasing frequency. To define the characteristics and outcomes of patients with double class-resistant disease, we retrospectively analyzed 17 patients who developed progressive disease (PD) on both TA classes for CLL (venetoclax, then BTKi, n=12; BTKi, then venetoclax, n=5). The cohort was heavily pre-treated (median lines of prior therapy: 4) and enriched for adverse disease genetics (complex karyotype: 12/12 tested, 100%; del(17p)/TP53 mutations: 15/17, 88%). The median time to progression on prior venetoclax was 24 (range 6-94) months, and on prior BTKi was 25 (range 1-55) months. Progression on second-line TA was manifest as progressive CLL in 11 patients and as Richter transformation in six. The median overall survival after progression on second-line TA was 3.6 (95%CI 2-11) months. Patients with double class-resistant CLL have a dismal prognosis, representing a group of high unmet need.
Concerted hepatoprotective effect of bradykinin potentiating factor and low dose of γ- radiation on Naja haje envenomed rats via Bax/Bcl2 pathway
This study investigates the concerted hepatoprotective effects for three doses of bradykinin potentiating factor (BPF) and/or followed by exposure to a low dose of γ-radiation (LDR) against Naja haje envenoming in rats. Male rats were injected with three consecutive doses of BPF (1μg/g i.p. for 3 days), followed by exposure to a low dose of gamma radiation (0.5 Gy), and then rats were injected with a dose of Naja haje venom (250 μg/kg i.p.).
- Results showed that Naja haje causes liver damage, significant elevation of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), cytochrome c, Nitric oxide (NO), malondialdehyde (MDA) and significant depletion in glutathione peroxidase (GPx) contents. In addition, significant depletion in B-cell lymphoma 2 (Bcl-2) and significant elevation in BcL-2 associated X (Bax protein), nuclear factor kappa B (NF-κB), interleukin-1β (IL-1β) in hepatocytes.
- Bradykinin potentiating factor and/or low dose of γ-radiation caused improvement in liver damage caused by Naja haje venom by a significant decrease in ALT, AST, ALP levels, Bax, cytochrome c, NF-κB, IL-1β, NO and MDA contents, BPF alone or combined with low dose radiation caused a significant increase in Bcl2 and GPx contents.In conclusion, the concerted impact of BPF and LDR may provide an effective venom detoxification tool that helps to reduce hepatic toxicity and extends the lifespan.
MYC, BCL2, and BCL6 expression as prognostic indicators in primary central nervous system lymphoma: A systematic review and meta-analysis
Background: We conducted a meta-analysis to comprehensively assess the predictive role of MYC, BCL2, and BCL6 genetic alterations and protein expression in PCNSL for clinical application.
Methods: A systematic retrieval was performed on PubMed, Embase, the Cochrane library, Web of Science, Scopus, and 2 Chinese databases. Cohort studies discussing the prognostic impact of MYC, BCl2, or BCL6 genetic alterations or gene expression in PCNSL were selected. The pooled hazard ratio (HR) and median survival ratio (MSR) were calculated.
Results: 31 studies involving 1739 patients fulfilled our inclusion criteria. MYC expression was significantly associated with short median OS (MSR = 0.62; 95%CI, 0.44-0.88) and PFS (HR = 1.53; 95%CI, 1.06-2.20). No significant association was found between BCL2 expression and OS or PFS (P > 0.05). BCL6 protein positivity was significantly associated with extended median OS (MSR = 1.62; 95%CI, 1.10-2.40).
MYC and BCL2 coexpression was significantly associated with short median OS (MSR = 0.61; 95%CI, 0.45-0.84). Subgroup analysis demonstrated that MYC protein positivity remained as a significant indicator for short median OS in studies whose sample size ≥ 45, treatment without WBRT, quality scale score ≥ 7, and positivity threshold set at 40% stratum (MSR < 1 and P < 0.05), but failed to reach a statistically significant difference in the other stratum.
Conclusions: MYC expression predicts inferior median OS and PFS in PCNSL. BCL6 protein positivity is associated with a favorable prognosis. The sample size, average age of subjects, WBRT treatment, study quality, and cut-off values for discriminating positive and negative protein expression in IHC may be origins of heterogeneity.
Keywords: BCL2; BCL6; Gene expression; MYC; Primary central nervous system lymphoma.

Synergistic melanoma cell death mediated by inhibition of both MCL1 and BCL2 in high-risk tumors driven by NF1/PTEN loss
Melanomas driven by loss of the NF1 tumor suppressor have a high risk of treatment failure and effective therapies have not been developed. Here we show that loss-of-function mutations of nf1 and pten result in aggressive melanomas in zebrafish, representing the first animal model of NF1-mutant melanomas harboring PTEN loss. MEK or PI3K inhibitors show little activity when given alone due to cross-talk between the pathways, and high toxicity when given together.
The mTOR inhibitors, sirolimus, everolimus, and temsirolimus, were the most active single agents tested, potently induced tumor-suppressive autophagy, but not apoptosis. Because addition of the BCL2 inhibitor venetoclax resulted in compensatory upregulation of MCL1, we established a three-drug combination composed of sirolimus, venetoclax, and the MCL1 inhibitor S63845. This well-tolerated drug combination potently and synergistically induces apoptosis in both zebrafish and human NF1/PTEN-deficient melanoma cells, providing preclinical evidence justifying an early-stage clinical trial in patients with NF1/PTEN-deficient melanoma.
BCL2 inhibitors and MCL1 inhibitors for hematological malignancies
BCL2 and MCL1 are commonly expressed pro-survival (anti-apoptotic) proteins in hematological cancers and play important roles in their biology either through dysregulation or by virtue of intrinsic importance to the cell-of-origin of the malignancy. A new class of small molecule anti-cancer drugs, BH3-mimetics, now enable specific targeting of these proteins in patients.
BH3-mimetics act by inhibiting the pro-survival BCL2 proteins to enable the activation of BAX and BAK, apoptosis effectors which permeabilize the outer mitochondrial membrane, triggering apoptosis directly in many cells and sensitizing others to cell death when combined with other anti-neoplastic drugs. Venetoclax, a specific inhibitor of BCL2, is the first approved in class, demonstrating striking single agent activity in chronic lymphocytic leukemia (CLL) and in other lymphoid neoplasms, as well as activity against acute myeloid leukemia (AML), especially when used in combination.
Key insights from the venetoclax experience include that responses occur rapidly, with major activity as monotherapy proving to be the best indicator for success in combination regimens. This emphasizes the importance of adequate single agent studies for drugs in this class. Furthermore, secondary resistance is common with long-term exposure and often mediated by genetic or adaptive changes in the apoptotic pathway, suggesting that BH3-mimetics are better suited to limited-duration, rather than continuous, therapy. The success of venetoclax has inspired development of BH3-mimetics targeting MCL1. Despite promising preclinical activity against MYC-driven lymphomas, myeloma and AML, their success may particularly depend on their tolerability profile given physiological roles for MCL1 in several non-hematological tissues.
![]() Recombinant Human Polyadenylate-Binding Protein-Interacting Protein 2 |
|||
7-05799 | CHI Scientific | 1mg | Ask for price |
![]() Polyadenylate-Binding Protein 2 (PABPN1) Antibody |
|||
20-abx004649 | Abbexa |
|
|
![]() Polyadenylate-Binding Protein 2 (PABPN1) Antibody |
|||
abx029099-400ul | Abbexa | 400 ul | EUR 627.6 |
![]() Polyadenylate-Binding Protein 2 (PABPN1) Antibody |
|||
abx029099-80l | Abbexa | 80 µl | EUR 343.2 |
![]() Polyadenylate-Binding Protein 2 (PABPN1) Antibody |
|||
20-abx217614 | Abbexa |
|
|
![]() Bovine Polyadenylate- binding protein 1, PABPC1 ELISA KIT |
|||
ELI-12383b | Lifescience Market | 96 Tests | EUR 1113.6 |
![]() Polyadenylate-Binding Protein-Interacting Protein 2 Protein |
|||
20-abx260556 | Abbexa |
|
|
![]() Polyadenylate-Binding Protein-Interacting Protein 2 Antibody |
|||
20-abx137383 | Abbexa |
|
|
![]() Embryonic polyadenylate-binding protein 2 Antibody / PABPN1L |
|||
F54625-0.08ML | NSJ Bioreagents | 0.08 ml | EUR 165 |
![]() Embryonic polyadenylate-binding protein 2 Antibody / PABPN1L |
|||
F54625-0.4ML | NSJ Bioreagents | 0.4 ml | EUR 379 |
![]() PAIP2 Polyadenylate-Binding Protein-Interacting protein 2 Human Recombinant Protein |
|||
PROTQ9BPZ3 | BosterBio | Regular: 25ug | EUR 380.4 |
Description: Recombinant Human PAIP2 produced in E.Coli is a single,non-glycosylated polypeptide chain containing 147 amino acids (1-127 a.a.) and having a molecular mass of 17.1 kDa.;PAIP2 human recombinant is fused to 20 amino acid His Tag at N-terminus and purified by convential chromatogrpahy techniques. |
![]() Polyadenylate-Binding Protein 1-Like 2 (PABPC1L2B) Antibody |
|||
abx030671-400ul | Abbexa | 400 ul | EUR 627.6 |
![]() Polyadenylate-Binding Protein 1-Like 2 (PABPC1L2B) Antibody |
|||
abx030671-80l | Abbexa | 80 µl | EUR 343.2 |
![]() Mouse Polyadenylate- binding protein 2, Pabpn1 ELISA KIT |
|||
ELI-35520m | Lifescience Market | 96 Tests | EUR 1038 |
![]() Human Polyadenylate- binding protein 2, PABPN1 ELISA KIT |
|||
ELI-21970h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Human Polyadenylate-binding protein 1 (PABPC1) |
|||
1-CSB-EP017352HU | Cusabio |
|
|
Description: Recombinant Human Polyadenylate-binding protein 1(PABPC1),partial expressed in E.coli |
![]() PABPC3 Antibody / Polyadenylate-binding protein 3 |
|||
F53970-0.05ML | NSJ Bioreagents | 0.05 ml | EUR 165 |
![]() Arabidopsis thaliana Polyadenylate-binding protein RBP47A (RBP47A) |
|||
1-CSB-EP522272DOA | Cusabio |
|
|
Description: Recombinant Arabidopsis thaliana Polyadenylate-binding protein RBP47A(RBP47A) expressed in E.coli |
![]() Polyadenylate-Binding Protein 4-Like (PABPC4L) Antibody |
|||
abx028778-400ul | Abbexa | 400 ul | EUR 627.6 |
![]() Polyadenylate-Binding Protein 4-Like (PABPC4L) Antibody |
|||
abx028778-80l | Abbexa | 80 µl | EUR 343.2 |
![]() Recombinant Human Polyadenylate-binding protein 1, His-SUMO, E.coli-100ug |
|||
QP6461-ec-100ug | EnQuireBio | 100ug | EUR 489.6 |
![]() Recombinant Human Polyadenylate-binding protein 1, His-SUMO, E.coli-10ug |
|||
QP6461-ec-10ug | EnQuireBio | 10ug | EUR 240 |
![]() Recombinant Human Polyadenylate-binding protein 1, His-SUMO, E.coli-1mg |
|||
QP6461-ec-1mg | EnQuireBio | 1mg | EUR 1958.4 |
![]() Recombinant Human Polyadenylate-binding protein 1, His-SUMO, E.coli-200ug |
|||
QP6461-ec-200ug | EnQuireBio | 200ug | EUR 760.8 |
![]() Recombinant Human Polyadenylate-binding protein 1, His-SUMO, E.coli-500ug |
|||
QP6461-ec-500ug | EnQuireBio | 500ug | EUR 1272 |
![]() Recombinant Human Polyadenylate-binding protein 1, His-SUMO, E.coli-50ug |
|||
QP6461-ec-50ug | EnQuireBio | 50ug | EUR 315.6 |
![]() Human Polyadenylate-Binding Protein 1 (PABPC1) ELISA Kit |
|||
abx259760-96tests | Abbexa | 96 tests | EUR 1093.2 |
![]() Human Polyadenylate- binding protein 3, PABPC3 ELISA KIT |
|||
ELI-43230h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Human Polyadenylate- binding protein 4, PABPC4 ELISA KIT |
|||
ELI-35673h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Mouse Polyadenylate- binding protein 1, Pabpc1 ELISA KIT |
|||
ELI-21806m | Lifescience Market | 96 Tests | EUR 1038 |
![]() Human Polyadenylate- binding protein 5, PABPC5 ELISA KIT |
|||
ELI-21807h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Human Polyadenylate- binding protein 1, PABPC1 ELISA KIT |
|||
ELI-12384h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Recombinant Transmembrane Protease Serine 2 Protein, Partial |
|||
E80016 | EpiGentek |
|
|
![]() Human Polyadenylate- binding protein 4- like, PABPC4L ELISA KIT |
|||
ELI-21969h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Human Polyadenylate- binding protein 1- like, PABPC1L ELISA KIT |
|||
ELI-14688h | Lifescience Market | 96 Tests | EUR 988.8 |
![]() Recombinant SARS-CoV-2 Spike Glycoprotein(S) (D614G), Partial |
|||
E80028 | EpiGentek |
|
|
![]() Bovine TNF alpha Recombinant |
|||
R00002-2 | BosterBio | 5ug/vial | EUR 310.8 |
Description: Tumor necrosis factor alpha (TNFSF2, TNF alpha) is a member of the TNF Superfamily. TNF alpha, being an endogenous pyrogen, is able to induce fever, to induce apoptotic cell death, to induce sepsis (through IL-1 & IL-6 production), to induce cachexia, induce inflammation, and to inhibit tumorigenesis and viral replication. Bovine TNF alpha Recombinant Protein is purified TNF alpha (TNFSF2) produced in yeast. |
![]() Bovine KIDNEY WHOLE 2 EA* |
|||
57120-2 | Pel-Freez | 2 EA | EUR 209.81 |
![]() SARS-CoV-2 Nucleocapsid Protein, Avi-His-tag |
|||
E80027 | EpiGentek |
|
|
![]() ELISA kit for Human Polyadenylate-binding protein 1-like (PABPC1L) |
|||
KTE61322-48T | Abbkine | 48T | EUR 398.4 |
Description: Quantitative sandwich ELISA for measuring Human Polyadenylate-binding protein 1-like (PABPC1L) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
![]() ELISA kit for Human Polyadenylate-binding protein 1-like (PABPC1L) |
|||
KTE61322-5platesof96wells | Abbkine | 5 plates of 96 wells | EUR 2538 |
Description: Quantitative sandwich ELISA for measuring Human Polyadenylate-binding protein 1-like (PABPC1L) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
![]() ELISA kit for Human Polyadenylate-binding protein 1-like (PABPC1L) |
|||
KTE61322-96T | Abbkine | 96T | EUR 646.8 |
Description: Quantitative sandwich ELISA for measuring Human Polyadenylate-binding protein 1-like (PABPC1L) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
![]() SARS-CoV-2 Spike S1 RBD Protein, Avi-His-tag |
|||
E80024 | EpiGentek |
|
|
![]() SARS-CoV-2 Spike S1 RBD Protein, Mouse Fc-fusion |
|||
E80026 | EpiGentek |
|
|
![]() SARS-CoV-2 Spike S1 (16-685) Protein, Avi-His-tag |
|||
E80021 | EpiGentek |
|
|
![]() SARS-CoV-2 Spike S1 RBD (V367F) Protein, Avi-His-tag |
|||
E80023 | EpiGentek |
|
|
![]() Recombinant Bovine Growth Hormone Binding Protein |
|||
CG042-100 | GenDepot | 100ug | EUR 740.4 |
![]() Recombinant Bovine Growth Hormone Binding Protein |
|||
CG042-101 | GenDepot | 1mg | EUR 3138 |
![]() Recombinant Bovine Growth Hormone Binding Protein |
|||
CG042-200 | GenDepot | 200ug | EUR 1048.8 |
![]() Recombinant Bovine Growth Hormone Binding Protein |
|||
7-00523 | CHI Scientific | 5µg | Ask for price |
![]() Recombinant Bovine Growth Hormone Binding Protein |
|||
7-00524 | CHI Scientific | 20µg | Ask for price |
![]() Recombinant Bovine Growth Hormone Binding Protein |
|||
7-00525 | CHI Scientific | 1mg | Ask for price |
![]() Recombinant TMPRSS2 Protein, Partial |
|||
E80017 | EpiGentek |
|
|
![]() SARS-CoV-2 Spike S1 (13-665) Protein, Fc Fusion, Avi-tag |
|||
E80020 | EpiGentek |
|
|
![]() SARS-CoV-2 Spike S1 (16-685) Protein, Fc Fusion, Avi-tag |
|||
E80022 | EpiGentek |
|
|
![]() SARS-CoV-2 Spike S1 RBD Protein, Human Fc-Fusion, Avi-Tag |
|||
E80025 | EpiGentek |
|
|
![]() Nori Bovine A1AT ELISA Kit-2 Plates |
|||
GR112012-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori Bovine A1PI ELISA Kit-2 Plates |
|||
GR112013-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori Bovine LDHA ELISA Kit-2 Plates |
|||
GR112014-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Human Polyadenylate-binding protein 1 (PABPC1) control (non-asymmetric methylated) peptide |
|||
AB-23051-CP | Alpha Diagnostics | 100ug | EUR 196.8 |
![]() Human Polyadenylate-binding protein 1 (PABPC1) control (PABPC1- asymmetric methylated) peptide |
|||
AB-23051-P | Alpha Diagnostics | 100ug | EUR 196.8 |
![]() Nori Bovine MMP-3 ELISA Kit (2 plates) |
|||
GR112027-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine BDNF ELISA Kit- 2 Plates |
|||
GR112038-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() GSI Bovine (cattle) UCP2 ELISA Kit (2 plates) |
|||
GR112039-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine HGF ELISA Kit- 2 Plates |
|||
GR112046-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Bovine Odorant-binding protein |
|||
1-CSB-MP362133BO | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in Mammalian cell |
![]() Bovine Odorant-binding protein |
|||
1-CSB-YP362133BO | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in Yeast |
![]() Bovine Odorant-binding protein |
|||
1-CSB-YP362133BOa0 | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in Yeast |
![]() Bovine Odorant-binding protein |
|||
1-CSB-YP362133BOa4 | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in Yeast |
![]() Bovine Odorant-binding protein |
|||
1-CSB-YP362133BOb0 | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in Yeast |
![]() Bovine Odorant-binding protein |
|||
1-CSB-BP362133BO | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in Baculovirus |
![]() Bovine Odorant-binding protein |
|||
1-CSB-EP362133BO | Cusabio |
|
|
Description: Recombinant Bovine Odorant-binding protein expressed in E.coli |
![]() Recombinant Human MMP-2 Protein |
|||
PROTP08253-2 | BosterBio | 10ug | EUR 380.4 |
Description: Matrix metalloproteinases (MMPs) are a family of endoproteases that require zinc and calcium for expressing catalytic activity. These enzymes play a central role in the maintenance and remodeling of the extracellular matrix. Elevated expression of their activity, caused either by up-regulation of their expression or down-regulation of their cognate inhibitors, has been implicated in various degenerative disorders, including arthritis, cardiovascular disease, skeletal growth-plate disorders, and cancer metastasis. MMP-2 is a secreted collagenase with specificity toward Type IV, V, VII, and X collagens. Recombinant human MMP-2 is a 62.0 kDa protein containing the entire catalytic N-terminal domain and the C-terminal domain (552 amino acids). |
![]() Recombinant Human TFF-2 Protein |
|||
PROTQ03403-2 | BosterBio | 20ug | EUR 380.4 |
Description: The Trefoil Factor peptides (TFF1, TFF2 and TFF3) are expressed in the gastrointestinal tract, and appear to play an important role in intestinal mucosal defense and repair. TFF2 has been shown to inhibit gastrointestinal motility and gastric acid secretion. Recent data suggests a potential role for TFF2 in acute and chronic asthma (Nikolaidis, N.M. et al. Am. Journal Respir. Cell Mol. Biol. (2003) 4: 458-464). Recombinant human TFF2 is a 12.0 kDa polypeptide of 107 amino acid residues, which includes a 40-amino acid trefoil motif containing three conserved intramolecular disulfide bonds. |
![]() Recombinant Human BD-2 Protein |
|||
PROTO15263-2 | BosterBio | 20ug | EUR 380.4 |
Description: Defensins (alpha and beta) are cationic peptides with a broad spectrum of antimicrobial activity that comprise an important arm of the innate immune system. The α-defensins are distinguished from the β-defensins by the pairing of their three disulfide bonds. To date, six human β-defensins have been identified; BD-1, BD-2, BD-3, BD-4, BD-5 and BD-6. β-defensins are expressed on some leukocytes and at epithelial surfaces. In addition to their direct antimicrobial activities, they can act as chemoattractants towards immature dendritic cells and memory T cells. The β-defensin proteins are expressed as the C-terminal portion of precursors and are released by proteolytic cleavage of a signal sequence and in some cases, a propeptide sequence. β-defensins contain a six-cysteine motif that forms three intra-molecular disulfide bonds. Recombinant human BD-2 is a 4.3 kDa protein containing 41 amino acid residues. |
![]() Recombinant Human Relaxin-2 Protein |
|||
PROTP04090-2 | BosterBio | 25ug | EUR 380.4 |
Description: Relaxin-2 is a peptide hormone structurally related to insulin, which is expressed in the placenta, decidua, prostate, and in the ovary during pregnancy. Of the three known relaxin genes, Relaxin-2 is the only relaxin known to circulate in the blood. Relaxin-2 binds specifically to the LGR7 and LGR8 receptors, previously identified as an “orphan” G protein coupled receptors. Signaling by Relaxin-2 through its target receptors enhances the growth of pubic ligaments and ripening of the cervix during birth. Recombinant Relaxin-2 is a nonglycosylated 6.0 kDa disulfide linked heterodimeric protein consisting of a 24 amino acid A-chain and a 29 amino acid B-chain. |
![]() Recombinant Murine IL-2 Protein |
|||
PROTP04351-2 | BosterBio | 20ug | EUR 380.4 |
Description: IL-2 is a powerful immunoregulatory lymphokine produced by T-cells in response to antigenic or mitogenic stimulation. IL-2/IL-2R signaling is required for T-cell proliferation and other fundamental functions which are essential for the immune response. IL-2 stimulates growth and differentiation of B-cells, NK cells, lymphokine activated killer cells, monocytes, macrophages and oligodendrocytes. Recombinant murine IL-2 is a 17.2 kDa protein, containing 149 amino acid residues. |
![]() Recombinant Human PAI-2 Protein |
|||
PROTP05120-2 | BosterBio | 10ug | EUR 380.4 |
Description: PAI-2 is an inhibitory serpin expressed mainly in keratinocytes, activated monocytes, and placental trophoblasts. It exists predominantly as a 47 kDa nonglycosylated intracellular protein which can be induced to be secreted as 60 kDa glycoprotein. The glycosylated and unglycosylated forms of PAI-2 are equally effective as inhibitors of urokinase-type plasminogen activator (uPA), the only established physiological target of this serpin. PAI-2 has a unique ability to form dormant polymers spontaneously and reversibly under physiological conditions. The physiological relevance of this property, which is neither a consequence of any mutation in the PAI-2 gene nor associated with any known disorder, is still unclear. However, it appears that the formation of intracellular dormant polymers may be important for the controlled release of the inhibitor from PAI-2 producing cells. Plasma levels of PAI-2 are usually low or undetectable, except during pregnancy and in some forms of monocytic leukemia. Secretion of PAI-2 from the placenta normally occurs during the third trimester of pregnancy and accounts for the dramatic increase in PAI-2 levels (up to 250 ng/ml), which are maintained at these levels until postpartum, and then rapidly decline. In addition to its vital role in protecting the placenta from degradation by uPA and/or uPA-activated proteases, PAI-2 has been shown to be essential for the prevention of metastatic spread of neck, lung and breast cancers. The beneficial effect of PAI-2 seen in these studies is presumed to stem from its ability to inhibit uPA-dependent cell dissemination. PAI-2 has also been reported to inhibit keratinocyte proliferation, and to participate in the innate immune response during viral infection. Recombinant human PAI-2 is a 415-residue nonglycosylated protein. |
![]() Mouse FGF-2 Recombinant Protein |
|||
R00121-2 | BosterBio | 5ug/vial | EUR 310.8 |
Description: FGF basic (FGF2) is a multipotential fibroblast growth factor that stimulates and supports proliferation, migration and differentiation. Mouse FGF basic (FGF-2) Recombinant Protein is purified FGF basic (FGF-2) produced in yeast. |
![]() Chicken IL-2 Recombinant Protein |
|||
R00387-2 | BosterBio | 5ug/vial | EUR 310.8 |
Description: Interleukin-2 (IL-2) is a cytokine produced by T-helper cells in response to antigenic or mitogenic stimulation. It is required for T-cell proliferation and other activities crucial to the regulation of the immune response. Chicken IL-2 Recombinant Protein is purified interleukin-2 produced in yeast. |
![]() BMP-2 Bone Morphogenetic Protein-2 Human Recombinant Protein, Monomer |
|||
PROTP12643-2 | BosterBio | Regular: 20ug | EUR 380.4 |
Description: Bone Morphogenetic Protein-2 Human Recombinant produced in E.Coli is a monomeric, non-glycosylated, Polypeptide chain containing 115 amino acids (283-396) and having a molecular mass of 13009 Dalton. ;The BMP-2 is purified by proprietary chromatographic techniques. |
![]() Nori® Bovine (cow) TLR3 ELISA Kit (2 plates) |
|||
GR106082-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP1 ELISA Kit (2 plates) |
|||
GR106213-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP2 ELISA Kit (2 plates) |
|||
GR106214-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP3 ELISA Kit (2 plates) |
|||
GR106215-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP4 ELISA Kit (2 plates) |
|||
GR106216-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP5 ELISA Kit (2 plates) |
|||
GR106217-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP6 ELISA Kit (2 plates) |
|||
GR106218-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP7 ELISA Kit (2 plates) |
|||
GR106219-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine (cow) BMP8a ELISA Kit (2 plates) |
|||
GR106220-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine IL-10 ELISA Kit (2 plates) |
|||
GR106295-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
![]() Nori® Bovine Erythropoietin R ELISA Kit (2 plates) |
|||
GR106439-2 | Genorise Scientific | 2 x 96-well | EUR 998.4 |
×