|
ORF cDNA clones
|
CRISPR / TALEN
|
Lentivirus
|
AAV
|
TALE-TF
|
ORF knockin clones
|
|
Antibody
|
Proteins
|
miRNA target clones
|
qPCR primers
|
shRNA clones
|
miRNA products
|
Promoter clones
|
Validated All-in-One™ qPCR Primer for CD5(NM_014207.3) Search again
Product ID:
HQP022337
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
LEU1, T1
Gene Description:
CD5 molecule
Target Gene Accession:
NM_014207.3(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Gene References into function
- CD5-negative regulation of B cell receptor signaling originates from tyrosine residue Y429 outside an immunoreceptor tyrosine-based inhibitory motif
- Origins and functions of B-1 cells with notes on the role of CD5. Review.
- multiple somatic mutations in human cancers. the value of the CD5 microsatellite as a marker for instability in different tumor types, particularly in B-cell leukemia and lymphoma.
- CD5 supports the survival of B cells by stimulating IL-10 production and by concurrently exerting negative feedback on BCR-induced signaling events that can promote cell death.
- CD5-negative, CD10-negative small B-cell leukemia: variant of chronic lymphocytic leukemia or a distinct entity
- CD5 is rapidly recruited at the immunological synapse (IS) and lowers the T cell response elicited by antigen presentation by targeting downstream signaling events without affecting IS formation.
- The CD5+ diffuse large-B-cell lymphoma (DLBCL) constitutes a disease category distinct from that of CD5- DLBCL and other CD5+ malignancies.
- the 5'-flanking region of human CD5 is transcriptionally active in T cells, and Ets transcription factors in conjunction with other regulatory elements are responsible for constitutive and tissue-specific CD5 expression
- Overexpression in these cells indicates diseaase progression in B=cell leukemia patients.
- CD5 is associated with receptor revision in activated mature B cells and likely to promote expression of suitable immunoglobulin gene receptors capable of initiating the germinal center reaction.
- The polymorphic CD5 promoter is associated with increased susceptibility to B-cell chronic lymphocytic leukemia and mantle cell lymphoma.
- balance between the 2 alternative exons 1 might be central to the regulation of membrane CD5 in human B cells
- analysis of CD5-positive diffuse large B-cell lymphoma with the unusual phenotype of cytoplasmic CD20 (+), surface CD20 (-) [case report]
- CD5 does not inhibit properly the BCR-mediated signaling in leukemic cells.
- T lymphocyte activation-induced cell death (AICD) in response to a cognate tumor is inversely proportional to the surface expression level of CD5.
- a decrease in CD22(+) B cells and increase in CD5(+)CD22(-) B cells play critical roles in the pathogenesis of RA mediated by the activation of B cells
- support a model where chronic lymphocytic leukemia cells are chronically stimulated, leading to CD5 activation and cell survival
- 3D solution structure of a non-glycosylated double mutant of the N-terminal domain of human CD5 was presented.
- CD5 positive diffuse large B-cell lymphoma frequently express BCL2 protein and show that it is mainly included in the non-germinal center B-cell type of this cancer.
- Report CD5-undetected by immunohistochemistry in a t(11;14)(q13;q32)-positive conjunctival mantle cell lymphoma. (case report)
- diminishes the threshold of the response by cells expressing CD5
- present results indicate that the CD5 lymphocyte receptor may sense the presence of conserved fungal components [namely, (1-->3)-beta-d-glucans] and support the therapeutic potential of soluble CD5 forms in fungal sepsis
