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C57BL/6JCya-Abl1em1/Cya
Common Name:
Abl1-KO
Product ID:
S-KO-16894
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
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Basic Information
Strain Name
Abl1-KO
Strain ID
KOCMP-11350-Abl1-B6J-VA
Gene Name
Abl1
Product ID
S-KO-16894
Gene Alias
Abl; E430008G22Rik; c-Abl
Background
C57BL/6JCya
NCBI ID
11350
Modification
Conventional knockout
Chromosome
2
Phenotype
MGI:87859
Document
Click here to download >>
Application
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Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Abl1em1/Cya mice (Catalog S-KO-16894) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000028190
NCBI RefSeq
NM_009594
Target Region
Exon 5~6
Size of Effective Region
~1.3 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Abl1, also known as Abelson murine leukemia viral oncogene homolog 1, is a key gene encoding a tyrosine kinase. It is involved in multiple cellular processes such as cell growth, differentiation, and adhesion through its participation in various signaling pathways [1-5].

In leukemia research, a translocation between chromosomes 9 and 22 leads to the formation of the constitutively active BCR-ABL1 oncoprotein, driving chronic myeloid leukemia (CML) [2-5]. Mutations in ABL1 kinase domain can confer resistance to ATP-competitive tyrosine kinase inhibitors (TKIs) used for CML treatment [1,2,3,4,5]. BCR-ABL1-like B-acute lymphoblastic leukemia/lymphoma, lacking the BCR-ABL1 translocation but having a similar gene expression pattern, may have alterations in the ABL class family of genes including ABL1, which determine sensitivity to tyrosine kinase inhibitors.

In conclusion, Abl1 is crucial for normal cellular functions through its kinase activity in signaling pathways. In the context of leukemia, understanding the role of Abl1, especially in the formation of BCR-ABL1 oncoprotein and associated drug resistance, has been significantly advanced through research. Insights from these studies have led to the development of targeted therapies like TKIs and investigational agents such as asciminib, aiming to improve treatment outcomes for leukemia patients [2-5].

References:

1. Réa, Delphine, Hughes, Timothy P. 2022. Development of asciminib, a novel allosteric inhibitor of BCR-ABL1. In Critical reviews in oncology/hematology, 171, 103580. doi:10.1016/j.critrevonc.2022.103580. https://pubmed.ncbi.nlm.nih.gov/35021069/

2. Leak, Steven, Horne, Gillian A, Copland, Mhairi. 2023. Targeting BCR-ABL1-positive leukaemias: a review article. In Cambridge prisms. Precision medicine, 1, e21. doi:10.1017/pcm.2023.9. https://pubmed.ncbi.nlm.nih.gov/38550948/

3. Manley, Paul W, Barys, Louise, Cowan-Jacob, Sandra W. 2020. The specificity of asciminib, a potential treatment for chronic myeloid leukemia, as a myristate-pocket binding ABL inhibitor and analysis of its interactions with mutant forms of BCR-ABL1 kinase. In Leukemia research, 98, 106458. doi:10.1016/j.leukres.2020.106458. https://pubmed.ncbi.nlm.nih.gov/33096322/

4. Amarante-Mendes, Gustavo P, Rana, Aamir, Datoguia, Tarcila Santos, Hamerschlak, Nelson, Brumatti, Gabriela. 2022. BCR-ABL1 Tyrosine Kinase Complex Signaling Transduction: Challenges to Overcome Resistance in Chronic Myeloid Leukemia. In Pharmaceutics, 14, . doi:10.3390/pharmaceutics14010215. https://pubmed.ncbi.nlm.nih.gov/35057108/

5. Branford, Susan, Fernandes, Adelina, Shahrin, NurHezrin, Shanmuganathan, Naranie, Wadham, Carol. . Beyond BCR::ABL1-The Role of Genomic Analyses in the Management of CML. In Journal of the National Comprehensive Cancer Network : JNCCN, 22, . doi:10.6004/jnccn.2023.7335. https://pubmed.ncbi.nlm.nih.gov/38394774/

Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
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