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Home >> Antibodies >> ALK Antibody / EML4-ALK Fusion Protein Antibody

ALK Antibody / EML4-ALK Fusion Protein Antibody [clone RM361] (R20381)

  Catalog No Formulation Size Price (USD)  
Image R20381-0.1ML Antibody in PBS with 50% glycerol, 1% BSA and 0.09% sodium azide 100 ul 439
Microvalidated Recrabbitmono
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ALK Antibody EML4-ALK Fusion WB. Western blot analysis of H2228 non-small cell lung carcinoma cell lysate using recombinant rabbit monoclonal clone RM361 demonstrates a distinct band near 80 kDa corresponding to EML4-ALK variant 3 fusion protein expression. The observed signal supports selective detection of clinically relevant ALK fusion-associated oncogenic kinase protein involved in lung adenocarcinoma-associated receptor tyrosine kinase signaling and precision oncology biomarker pathways.
Availability 1-3 business days
Species Reactivity Human
Format Purified
Host Rabbit
Clonality Recombinant Rabbit Monoclonal
Isotype Rabbit IgG
Clone Name RM361
Purity Protein A purified from animal origin-free supernatant
UniProt Q9UM73
Localization Cytoplasmic, nuclear
Applications Western Blot : 1:1000-1:2000
Limitations This ALK Antibody / EML4-ALK Fusion Protein Antibody is available for research use only.
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Description

Anaplastic lymphoma kinase (ALK) is a receptor tyrosine kinase belonging to the insulin receptor superfamily that functions in neuronal development, intracellular signaling, and cellular differentiation pathways. ALK Antibody / EML4-ALK Fusion Protein Antibody recognizes total ALK protein including oncogenic ALK fusion proteins associated with constitutive kinase activation and tumor progression in multiple malignancies.

ALK antibody, also referred to as EML4-ALK antibody and Anaplastic lymphoma kinase antibody in the literature, is widely used in molecular oncology, precision medicine, and targeted therapy research applications. Recombinant rabbit monoclonal clone RM361 was generated against a peptide corresponding to the C-terminus of human ALK, supporting detection of both native ALK and clinically relevant ALK fusion proteins.

ALK rearrangements are among the most significant oncogenic driver events identified in non-small cell lung carcinoma (NSCLC), particularly lung adenocarcinoma. The most extensively characterized ALK rearrangement involves fusion between echinoderm microtubule-associated protein-like 4 (EML4) and ALK, generating constitutively active EML4-ALK fusion kinases capable of driving persistent downstream signaling independent of normal receptor regulation. These fusion proteins activate proliferative and survival-associated pathways including MAPK, PI3K-AKT, JAK-STAT, and PLCgamma signaling cascades.

EML4-ALK fusion-positive tumors represent clinically actionable molecular subsets associated with sensitivity to ALK-targeted kinase inhibitors. Consequently, ALK fusion detection has become highly important in precision oncology and translational cancer research. Multiple EML4-ALK fusion variants have been identified, each characterized by distinct breakpoint structures and biologic properties influencing oncogenic signaling and therapeutic response patterns.

Western blot analysis using clone RM361 demonstrates detection of EML4-ALK variant 3 in the NSCLC cell line H2228, supporting recognition of clinically relevant ALK fusion-associated protein species. The observed band near approximately 80 kDa is consistent with expression of the EML4-ALK fusion protein rather than full-length native ALK receptor, reflecting the altered molecular architecture generated by chromosomal rearrangement-associated fusion events.

In addition to NSCLC, ALK fusion-associated oncogenic signaling has been implicated in anaplastic large cell lymphoma, inflammatory myofibroblastic tumor, neuroblastoma, and additional malignancies. Persistent kinase activation resulting from ALK rearrangement promotes malignant transformation, survival signaling, migratory behavior, and therapy-responsive oncogenic dependency states.

Because ALK fusion proteins are central drivers of tumor-associated kinase signaling and molecularly targeted therapeutic strategies, antibodies capable of detecting EML4-ALK-associated protein expression remain valuable tools in translational oncology and biomarker-focused research applications. Clone RM361 supports investigation of fusion-associated kinase biology and oncogenic ALK pathway activation within molecularly defined cancer systems.

Together, the available western blot data support the use of ALK antibody clone RM361 for investigating EML4-ALK fusion-associated oncogenic signaling, receptor tyrosine kinase activation, and precision oncology-associated molecular pathways.

For additional ALK and oncogenic kinase research antibodies targeting fusion protein signaling, lung cancer biomarkers, and lymphoma-associated receptor tyrosine kinase pathways, explore the broader ALK Antibody page featuring recombinant rabbit monoclonal clone ALK1/6698R.

Application Notes

The stated application concentrations are suggested starting points. Titration of the ALK Antibody / EML4-ALK Fusion Protein Antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Immunogen

A peptide corresponding to the C-terminus of human ALK (Anaplastic lymphoma kinase) was used as the immunogen for the recombinant ALK antibody.

Storage

Store the recombinant ALK antibody at -20oC.

Alternate Names

ALK antibody, EML4-ALK antibody, Anaplastic lymphoma kinase antibody, ALK fusion protein antibody, EML4-ALK fusion protein antibody

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