apl-1 Antibody

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Description

Definition and Target Overview

apl-1 Antibody refers to antibodies targeting the amyloid precursor-like protein 1 (APL-1 or APLP-1), a transmembrane metalloprotein involved in neuronal development, synaptic function, and intracellular trafficking. APL-1 is a homolog of the amyloid precursor protein (APP) and is conserved across species, including humans (Homo sapiens) and the nematode Caenorhabditis elegans .

Biological Role of APL-1

APL-1 regulates critical processes in neurons:

  • Synaptic Transmission: APL-1 modulates synaptic function, as shown in C. elegans studies where knockdown of apl-1 led to hypersensitivity to the acetylcholinesterase inhibitor aldicarb, indicating defects in neurotransmission .

  • Axon Regeneration: APL-1 inhibits axon regeneration in mature neurons, acting through its extracellular E2 domain .

  • Intracellular Trafficking: APL-1 trafficking depends on small GTPases like RAB-5 and UNC-108, which regulate its expression in neurons .

Applications of APL-1 Antibodies

Antibodies against APL-1 are widely used in research for:

ApplicationDetails
Western BlotDetects APL-1 in lysates (e.g., human brain tissue) at ~119 kDa under reducing conditions .
ImmunohistochemistryLocalizes APL-1 to neuronal cytoplasm in human brain sections (e.g., cortex, hippocampus) .
ImmunocytochemistryIdentifies APL-1 in cell lines (e.g., SH-SY5Y neuroblastoma cells) .
Functional StudiesInvestigates APL-1’s role in synaptic defects, axon regeneration, and neurodegeneration .

Synaptic Function in C. elegans

  • Knockdown Effects: RNAi-mediated suppression of apl-1 causes aldicarb hypersensitivity, rescued by transgenic expression of full-length APL-1 in a dose-dependent manner .

  • Genetic Interactions: APL-1 expression is regulated by kinesins (UNC-104, UNC-116) and GTPases (RAB-5, UNC-108), linking it to vesicle transport pathways .

Axon Regeneration Inhibition

  • APL-1 restricts axonal regrowth post-injury in C. elegans GABAergic motor neurons.

  • The E2 domain of APL-1 is essential for this inhibitory function, independent of its cytoplasmic domain .

Human APLP-1 Expression

  • APLP-1 is highly expressed in human neuronal tissues (e.g., brain cortex) and cancer cell lines (e.g., TT medullary thyroid cancer cells) .

  • Antibody validation in human samples confirms specificity for cytoplasmic APLP-1 .

Clinical and Preclinical Relevance

  • Neurological Disorders: APL-1’s role in synaptic function and axon repair links it to neurodegenerative diseases (e.g., Alzheimer’s) .

  • Cancer Research: APLP-1 is overexpressed in certain cancers (e.g., neuroblastoma), making it a potential biomarker .

Challenges and Future Directions

  • Mechanistic Insights: The exact pathways through which APL-1 regulates synaptic plasticity and regeneration remain unclear.

  • Therapeutic Potential: Targeting APL-1’s E2 domain could offer strategies to enhance axon repair in neurological injuries .

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
apl-1 antibody; C42D8.8Amyloid-beta-like protein antibody
Target Names
apl-1
Uniprot No.

Target Background

Function
APL-1 is a crucial protein essential for normal developmental progression throughout all life stages of the organism. Its role is particularly prominent during the molting stage, where it is required for larval transitions and morphogenesis. APL-1 collaborates with heterochronic genes, including members of the let-7 family, to regulate the transition from larval stage to adulthood. It also acts synergistically with acn-1 in let-7-regulated postembryonic cell division of hypodermal seam cells. Moreover, APL-1 influences multiple pathways, including daf-12 and daf-16 activity, to modulate physiological and reproductive processes such as body size and egg-laying. There is evidence suggesting a potential role of APL-1 in neurotransmission.
Gene References Into Functions
  1. Research suggests that APL1-D2 binds Cu(I) and Cu(II) with insufficient strength to sustain catalysis, indicating that it does not play a significant role in copper handling in C. elegans. PMID: 24276282
  2. Hypothetical models have been proposed to elucidate how sAPL-1 signaling influences metabolic and developmental pathways. PMID: 23044509
  3. [review] Both loss and overexpression of APL-1 result in lethality, highlighting the importance of maintaining homeostatic levels of APL-1, particularly within neurons. PMID: 22038715
  4. Pan-neuronal expression of APL-1, the Caenorhabditis elegans ortholog of APP, disrupts several behaviors, including olfactory and gustatory learning behavior and touch habituation. PMID: 22836251
  5. Signaling of the released APL-1 fragment modulates multiple metabolic states, underscoring the requirement for APL-1 throughout development. PMID: 22466039
  6. Cholesterol and lrp-1 are implicated in the regulation of synaptic transmission, similar to apl-1. PMID: 22363792
  7. A critical cis-regulatory element of apl-1 transcription has been identified. PMID: 21150118
  8. Loss of apl-1 leads to neurotransmission defects. PMID: 20862215
  9. The x-ray structure of the E2 domain of APL-1 has been elucidated. PMID: 19906646
  10. The 5' UTR of the Aplp1 gene lacks any type of CAGA box. PMID: 15208260
  11. APL-1 functions non-cell-autonomously during development. PMID: 17267616
  12. apl-1 expression is upregulated during the last larval stage in hypodermal seam cells, a process that is transcriptionally regulated by hbl-1, lin-41, and lin-42. PMID: 18262516

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Database Links

KEGG: cel:CELE_C42D8.8

STRING: 6239.C42D8.8a.2

UniGene: Cel.6164

Protein Families
APP family
Subcellular Location
Membrane; Single-pass type I membrane protein. Early endosome.
Tissue Specificity
Expressed in the head, pharynx, spermatheca, uterus, vulva, tail and ventral neurons. Specifically expressed in nerve ring interneurons, the ventral cord, socket and amphids in the head, with strong expression in junctional cells, including the pharyngeal

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