Human Tyrosine-Protein Kinase ABL1 (ABL1) Protein (Active)

Este producto es parte de ABL - Tyrosine-protein kinase ABL
Human Tyrosine-Protein Kinase ABL1 (ABL1) Protein (Active)
780€ (20 µg)

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Name
Human Tyrosine-Protein Kinase ABL1 (ABL1) Protein (Active)
Category
Proteins and Peptides
Provider
Abbexa
Reference
abx693110
Tested Applications
SDS-PAGE

Description

Tyrosine-Protein Kinase ABL1 (ABL1) protein is a recombinant Human protein expressed in Insect.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Proteins and Peptides
Immunogen Target
Tyrosine-Protein Kinase ABL1 (ABL1)
Host
Insect
Assay Type
Activity: Active
Sequence Fragment: Pro137-Ser554
Tag: N-terminal GST tag
Origin
Human
Observed MW
74 kDa
Expression
Recombinant
Purity
> 75% (SDS-PAGE)
Size 1
20 µg
Size 2
50 µg
Form
Liquid
Tested Applications
SDS-PAGE
Buffer
50 mM Tris, 100 mM NaCl, 0.5 mM PMSF, 0.5 mM EDTA, 0.5 mM Reduced Glutathione, pH 8.0.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
Shelf Life: 6 months.
Dry Ice
No
UniProt ID
P00519
Gene ID
25
NCBI Accession
NP_009297.2
OMIM
189980
Alias
ABL,BCR-ABL,CHDSKM,ABL proto-oncogene 1 non-receptor tyrosine kinase
Background
Protein ABL1
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.
Endotoxin Level: < 1.0 EU per µg (LAL method).

Background

ABL1 is a non-receptor tyrosine kinase involved in various cellular processes, including cytoskeletal remodeling, cell migration, DNA damage response, and signal transduction. It is ubiquitously expressed and localized in both the nucleus and cytoplasm, where it interacts with numerous signaling proteins. ABL1 contains SH2 and SH3 domains, a kinase domain, and regulatory regions that facilitate its interaction with other proteins and its activation in response to cellular stimuli. Dysregulation of ABL1, particularly through chromosomal translocations such as the Philadelphia chromosome, results in the BCR-ABL1 fusion protein, which drives chronic myeloid leukemia (CML) by promoting uncontrolled cell proliferation and survival. Targeting ABL1 with tyrosine kinase inhibitors, such as imatinib, has revolutionized the treatment of CML and highlighted its role as a key therapeutic target. Beyond cancer, ABL1 contributes to cellular responses to oxidative stress, DNA damage repair, and cytoskeletal dynamics, underscoring its importance in maintaining cellular homeostasis and responding to environmental challenges.

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