RAT ANTI MOUSE CD34 Biotin

Price:
179 EUR
214 USD
148 GBP
known as: RAT ANTI MOUSE CD34 Biotin
Catalog number: genta-ABS0643
Product Quantity: 0.1 mg
Category:
Supplier: AbD

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Gene target: cd34

Related genes to: RAT ANTI MOUSE CD34 Biotin

Symbol : biotin NIH gene
LocusTag : Bathy11g00270
chromosome : 11
description : biotin synthase
type of gene : protein-coding
Modification date : 2015-06-26
Symbol : CD34 NIH gene
dbXrefs : Ensembl:ENSLACG00000018825
chromosome : Un
description : CD34 molecule
type of gene : protein-coding
Modification date : 2016-03-29

Related Pathways to: RAT ANTI MOUSE CD34 Biotin

Gene about :CD34
Pathway :Bt Hematopoietic Stem Cell Differentiation
CD34
Gene about :biotin
Pathway :Sc Protein Modifications
biotin

Related product to: RAT ANTI MOUSE CD34 Biotin

Related Articles about: RAT ANTI MOUSE CD34 Biotin

The influence of temperature treatment before cryopreservation on the viability and potency of cryopreserved and thawed CD34(+) and CD45(+) cord blood cells.

Hematopoietic stem cell (HSC) viability and potency is crucial for qualified cord blood (CB) transplants. This study analyzes time and temperature condition before cryopreservation for the viability of CD34(+)/CD45(+) cells after cryopreservation. - Source :PubMed

[Effect of MicroRNA-214 on Migration of Cord Blood CD34(+) Cells Induced by Bone Marrow Mesenchymal Stem Cells].

To investigate the possible effect of MicroRNA-214 (miR-214) on migration of umbilical cord blood CD34(+) hematopoietic stem/progenitor cells induced by BM-MSC. - Source :PubMed

[Prostaglandin E2 Receptor 4 Agonist Promotes Human CD34(+) Cell Proliferation in vitro by Activating Wnt/β-Catenin Signaling Pathway].

To investigate the potential signaling pathway that regulates the proliferation of human CD34(+) cells stimulated by prostaglandin E2 receptor 4 agonist (EP4A) in vitro. - Source :PubMed

Cutaneous and Superficial Soft Tissue CD34(+) Spindle Cell Proliferation.

- Cutaneous and superficial soft tissue spindle cell proliferations with CD34 expression represent a unique heterogeneous group of lesions. They can pose diagnostic challenges for unaware pathologists in their daily practice. - Source :PubMed

The effect of CD34(+) cell telomere length and hTERT expression on the outcome of autologous CD34(+) cell transplantation in patients with chronic heart failure.

Age-related telomere attrition in stem/progenitor cells may diminish their functional capacity and thereby impair the outcome of cell-based therapies. The aim of the present study was to investigate the effect of CD34(+) cell telomere length and hTERT expression on the clinical outcome of autologous CD34(+) cell transplantation. We studied 43 patients with cardiomyopathy. Their peripheral blood CD34(+) cells were mobilized with granulocyte colony-stimulating factor, enriched by immunoselection and delivered transendocardially. Relative telomere length and expression levels of hTERT were measured using a real-time PCR assay. Immunoselected CD34(+) cells had longer telomere length compared to leukocytes in leukapheresis products (p=0.001). In multivariate analysis, CD34(+) cell telomere length was not associated with the clinical outcome (b=3.306, p=0.540). While hTERT expression was undetectable in all leukapheresis products, 94.4% of the CD34(+) enriched cell products expressed hTERT. Higher CD34(+)hTERT expression was associated with a better clinical outcome on univariate analysis (b=87.911, p=0.047). Our findings demonstrate that CD34(+) cell telomere length may not influence the clinical outcome in cardiomyopathy patients treated with autologous CD34(+) cell transplantation. Larger studies are needed to validate the impact of the CD34(+)hTERT expression on the clinical outcome of autologous CD34(+) cell transplantation. - Source :PubMed

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