Chronic Lymphocytic Leukemia FISH Probes
Chronic Lymphocytic Leukemia (CLL) FISH probes are specialized research tools designed to detect genetic abnormalities associated with CLL, a common type of leukemia in adults. Utilizing fluorescence in situ hybridization (FISH) technology, these probes allow researchers to identify critical chromosomal alterations, such as deletions on chromosomes 13q, 11q, and 17p, which are significant for prognosis and treatment decisions. Our FISH probes provide essential insights into the genetic landscape of CLL, facilitating a deeper understanding of its biology and contributing to the development of targeted therapeutic strategies for improved patient management.
Description: Labeled FISH probes as chromosomal markers using FISH Technique.
Description: Labeled FISH probes as chromosomal markers using FISH Technique.
Description: The ATM probe is a 500 kb unique sequence probe that hybridizes to the 11q22.3 region of chromosome ...
Description: The BCL2 (18q21) Break probe is optimized to detect translocations involving the BCL2 gene region ...
Description: These fluorescence in situ hybridization (FISH) probes are intended to detect the t(11;14)(q13;q32) ...
Description: This MYB Probe is intended to detect the copy number of the LSI MYB probe target located at ...
Description: The 6q21 FISH Probee is designed to hybridize to 229 kb of the 6q21 region of chromosome 6.
Description: The BIRC3 FISH Probe from Creative Bioarray is designed to detect the human BIRC3 gene located on ...
Description: The TP53 FISH Probe from Creative Bioarray is designed to detect the human TP53 gene located on ...
Description: The chromosomal region 12q13-q15 is often affected by translocations and amplifications in soft ...
Description: The RB1(13q14) Probe contains unique DNA sequences specific to the RB1 gene within the 13q14 region ...
Description: D13S319/LAMP1 FISH Probe is meticulously designed to identify copy number variations in the LAMP1 ...