Taiy Chemical
Hemokinin 1 (human)
Synonym HK1
Species Human
Protein Accession Q96A04
Purity Greater than 95% as determined by SDS-PAGE
Endotoxin Level Less than 1 EU/ug
Biological Activity Fully biologically active when compared to standard. The ED50 as determined by a cell proliferation assay using human TF-1 cells is less than 10 ng/ml, corresponding to a specific activity of > 1.0 × 10^5 IU/mg.
Expression System Baculovirus-Infected Sf9 Insect Cells
Fusion Tag None
Predicted Molecular Mass Approximately 4.1 kDa
Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA
Reconstitution It is recommended to reconstitute the lyophilized Hemokinin 1 in sterile 18MΩ-cm H2O not less than 100 µg/ml, which can then be further diluted to other aqueous solutions.
Storage & Stability Lyophilized Hemokinin 1 although stable at room temperature for 3 weeks, should be stored desiccated below -18°C. Upon reconstitution HK1 should be stored at 4°C between 2-7 days and for future use below -18°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Avoid repeated freeze-thaw cycles.
FAQ
What is Hemokinin 1 (human) and what role does it play in the human body?

Hemokinin 1 is a peptide belonging to the tachykinin family, which is a group of neuropeptides best known for their role in neurotransmission. Structurally, Hemokinin 1 is similar to other tachykinins like Substance P, which has been extensively studied for its involvement in inflammatory processes and pain perception. Hemokinin 1 is encoded by the TAC4 gene in humans and is expressed in various tissues, including the immune system and reproductive organs. Historically, much attention in research was given to Substance P and similar tachykinins, but recent studies have shined light on the distinctive roles of Hemokinin 1, suggesting its unique actions apart from traditional tachykinins.

The potential functions of Hemokinin 1 in the body are diverse. One crucial role is in the modulation of immune responses. Hemokinin 1 appears to influence the balance and activities of immune cells, including macrophages and lymphocytes. By acting on these cells, Hemokinin 1 may mediate pro-inflammatory and anti-inflammatory responses, which are vital for the body's ability to respond to infections and injuries. It also plays a role in the sensory nervous system. The peptide can influence nociception, or the sensory nervous system's response to pain, suggesting that Hemokinin 1 could be involved in regulating pain thresholds and responses.

Furthermore, research indicates that Hemokinin 1 might impact vasodilation and vasoconstriction, the processes by which blood vessels widen and narrow respectively. This suggests a possible role in cardiovascular regulation, where it could affect blood pressure and flow. In reproductive biology, Hemokinin 1 might also be important, given its expression in reproductive tissues and potential involvement in reproductive processes, although this area requires further exploration.

Overall, Hemokinin 1 represents an intriguing peptide with multiple physiological roles potentially extending into immune modulation, sensory processing, cardiovascular health, and reproductive biology. Understanding Hemokinin 1 better could offer insights into novel therapeutic targets for conditions such as chronic inflammatory diseases, pain management issues, and even cardiovascular disorders. Continued research will likely reveal more about its complex roles and applications in human health.

How does Hemokinin 1 (human) differ from other related peptides such as Substance P?

Hemokinin 1 and Substance P, while sharing membership within the tachykinin family, exhibit both structural similarities and functional distinctions that highlight their unique roles in human physiology. Structurally, both peptides share a common C-terminal sequence that is characteristic of tachykinins, yet they are encoded by different genes— Hemokinin 1 by the TAC4 gene, whereas Substance P by the TAC1 gene. This structural similarity is crucial because it dictates their ability to bind particular receptor subtypes, primarily the neurokinin-1 (NK1) receptor. However, despite some overlap in receptor interaction, Hemokinin 1 and Substance P have distinct affinities and signaling capabilities, contributing to their divergent roles in various biological processes.

One of the notable differences is in their expression and functional implications in different tissues. While Substance P is predominantly found in the central and peripheral nervous systems and is heavily involved in pain perception and inflammatory responses, Hemokinin 1 has a broader expression, notably within the immune system and certain peripheral tissues. Hemokinin 1's significant role within the immune system highlights its potential involvement in modulating immune responses, where it may regulate activities of immune cells like macrophages and lymphocytes—an aspect less pronounced with Substance P.

Moreover, these peptides differ in their contributions to physiological and pathophysiological processes. Hemokinin 1 has shown unique immunological roles, potentially impacting conditions involving immune dysregulation. In contrast, Substance P is widely recognized for its contributions to neurogenic inflammation and pain pathways, where it facilitates the release of pro-inflammatory cytokines and mediates the response to acute pain stimuli.

Hemokinin 1 may also influence vascular and reproductive systems differently compared to Substance P. Early studies suggest Hemokinin 1 might play a role in vascular regulation by affecting blood vessel constriction and dilation, thereby potentially influencing blood pressure and flow. Additionally, its presence in reproductive tissues hints at possible roles in reproductive physiology and pathology, although these areas require further research.

Collectively, while Hemokinin 1 and Substance P are both integral to body function, their distinct gene origins, patterns of expression, and specific biological roles allow them to contribute uniquely to health and disease. These differences open avenues for targeted therapeutic strategies focusing on Hemokinin 1 for immune-related conditions or Substance P for managing pain and inflammation, reflecting their specialized yet overlapping roles within the tachykinin family.

In what research areas is Hemokinin 1 (human) currently being studied, and what potential applications may arise from these studies?

Hemokinin 1 is currently a focus of research in several fields due to its broad potential applications in human health and disease management. One key area of investigation is the immune system, where researchers are exploring Hemokinin 1's role in modulating immune responses. This peptide is thought to influence the activity of immune cells such as lymphocytes and macrophages, which are crucial for maintaining immune homeostasis and fighting infections. Understanding Hemokinin 1's exact role and mechanisms in the immune system could lead to new therapeutic approaches for autoimmune diseases, allergies, and other immune-related disorders by modulating immune cell behavior to achieve desired outcomes.

Another significant area of study is pain management. Hemokinin 1 has been implicated in nociception, the sensory process that provides the signals that lead to pain. By elucidating the specific pathways through which Hemokinin 1 contributes to pain perception and modulation, researchers aim to develop novel analgesic drugs that could provide relief for chronic pain sufferers without the side effects associated with many current pain medications. This could have profound implications for millions of individuals experiencing chronic pain and could significantly enhance quality of life.

In addition to immune and pain research, Hemokinin 1 is being investigated for its role in cardiovascular health. Preliminary studies suggest that Hemokinin 1 may influence blood vessel tone and, consequently, blood pressure regulation. This line of research could pave the way for new treatments for hypertension and related cardiovascular disorders, potentially reducing the risk of associated complications such as stroke and heart disease by targeting pathways involving Hemokinin 1.

Reproductive health is another intriguing research area where Hemokinin 1 is being explored. Given its expression in reproductive tissues, scientists are investigating its potential roles in fertility, pregnancy, and reproductive health disorders. Understanding these roles could lead to innovations in reproductive medicine, including fertility treatments and interventions for reproductive system disorders.

Finally, Hemokinin 1 is also being studied in the context of cancer research. Some findings suggest that it may be involved in tumor progression or suppression, although the mechanisms remain to be fully understood. This could eventually lead to novel cancer therapies that exploit Hemokinin 1's interactions within the tumor microenvironment, offering new hope for treatment strategies.

Overall, the ongoing research into Hemokinin 1 is poised to significantly expand our understanding of this peptide and its wider implications. Each of these research areas holds promise not only for advancing scientific knowledge but also for developing innovative treatments that could profoundly impact various aspects of human health, addressing unmet medical needs and providing new care options for patients worldwide.

What are the potential therapeutic benefits of targeting Hemokinin 1 (human) in medical treatments?

Targeting Hemokinin 1 in medical treatments presents several potential therapeutic benefits owing to its distinctive roles in various physiological processes. One of the most promising applications lies in the area of immunotherapy. Given Hemokinin 1's involvement in modulating immune responses, it represents a potential target for conditions that involve immune system dysregulation, such as autoimmune diseases and chronic inflammatory conditions. By targeting pathways associated with Hemokinin 1, it may be possible to develop treatments that effectively balance immune responses, reducing pathological inflammation while still allowing the immune system to function adequately.

In the realm of pain management, Hemokinin 1 offers a novel therapeutic target distinct from traditional pain relief mechanisms. Its involvement in nociceptive pathways—those associated with the sensation of pain—suggests that modulating Hemokinin 1's activity could help in managing chronic pain conditions. Current pain medications, such as opioids, have significant drawbacks, including addiction potential and severe side effects. By developing drugs that specifically target Hemokinin 1 pathways, it may be possible to achieve effective pain relief with fewer adverse effects, providing a safer alternative for patients with chronic pain.

Furthermore, cardiovascular health is another area where Hemokinin 1 targeted therapies might prove beneficial. If ongoing research confirms its role in regulating blood pressure through effects on vasodilation and vasoconstriction, Hemokinin 1 could become a target for managing hypertension and preventing its complications. This approach could lead to therapies that offer more precise regulation of vascular function and better cardiovascular outcomes, augmenting current treatment options.

Additionally, targeting Hemokinin 1 might have implications for reproductive health and fertility treatments. Since Hemokinin 1 is expressed in reproductive tissues, therapies involving this peptide could explore ways to enhance or regulate reproductive processes, addressing infertility issues or disorders related to reproductive health. This could open new pathways in reproductive medicine and offer additional therapeutic strategies for individuals seeking reproductive assistance.

Finally, in oncology, understanding Hemokinin 1's potential role in cancer biology could lead to innovative treatment regimens. If Hemokinin 1 influences tumor growth or metastatic behavior, it could become a target for cancer therapies, either independently or in conjunction with current treatment modalities. Such therapies could be aimed at disrupting tumor-promoting pathways specific to Hemokinin 1, potentially hindering cancer progression and improving survival rates.

Overall, targeting Hemokinin 1 represents an exciting frontier with the potential to impact various aspects of medical treatment. The diversity of processes that Hemokinin 1 is involved in—ranging from immune modulation and pain management to cardiovascular, reproductive, and cancer biology—suggests that advances in targeting this peptide could yield significant therapeutic breakthroughs. Achieving these advances will require a deeper understanding of Hemokinin 1's specific roles and mechanisms, but the potential benefits for patient care and treatment options are substantial.

How is Hemokinin 1 (human) studied in laboratory settings, and what methodologies are used to explore its functions?

Studying Hemokinin 1 in laboratory settings involves a variety of sophisticated methodologies designed to elucidate its complex roles and actions in the human body. One of the foundational approaches to studying Hemokinin 1 is through molecular and cellular biology techniques. This involves analyzing the expression patterns of Hemokinin 1 at the genetic level. Researchers use quantitative polymerase chain reaction (qPCR) and RNA sequencing to assess the expression of the TAC4 gene, which encodes Hemokinin 1, in different tissues under varying conditions. These techniques provide a basis for understanding where Hemokinin 1 is produced and potentially active, offering insights into its physiological and pathophysiological roles.

Further, researchers often employ in vitro studies using cultured cells to investigate Hemokinin 1's effects on specific cell types. This might involve adding synthetic Hemokinin 1 to cultures of immune cells, such as macrophages or lymphocytes, to observe changes in cell behavior, signaling pathways, or immune responses. Cell cultures provide a controlled environment to dissect the cellular mechanisms by which Hemokinin 1 operates. Biochemical assays, such as enzyme-linked immunosorbent assays (ELISA) for protein quantification, or Western blotting for protein detection, are frequently utilized to quantify Hemokinin 1 and its receptors or evaluate downstream signaling molecules influenced by its activity.

Animal models represent another critical methodology in studying Hemokinin 1. Genetically modified mice, for example, with overexpression or deletion of TAC4, are used to assess Hemokinin 1’s physiological effects and its role in disease models. These animal studies are invaluable for understanding the in vivo functions of Hemokinin 1, including its impact on systemic immune responses, pain perception, cardiovascular function, and reproductive processes. The insights garnered from these models contribute significantly to our understanding of how Hemokinin 1 might be leveraged therapeutically in humans.

Advanced imaging techniques also contribute to the study of Hemokinin 1. Techniques such as immunohistochemistry facilitate visualizing Hemokinin 1 within tissues, helping to reveal its spatial distribution and potential sites of action. Additionally, cutting-edge methodologies like optogenetics and CRISPR gene editing are being explored to precisely manipulate Hemokinin 1 pathways, either by controlling its expression or altering receptor interactions, to better understand its biological roles and therapeutic potentials.

Finally, proteomics and bioinformatics offer new frontiers in analyzing the interactions of Hemokinin 1 with other proteins and its impact on broader biological networks. These technologies can uncover novel pathways influenced by Hemokinin 1 and identify potential cross-talk with other signaling molecules, thereby expanding our comprehension of its role in health and disease.

Collectively, these diverse laboratory approaches provide a comprehensive toolkit for dissecting the multifaceted nature of Hemokinin 1, offering insights that could eventually lead to the development of targeted therapies across multiple medical fields, from immunology and pain management to cardiovascular and reproductive health. The continuous advancement in these methodologies promises to deepen our understanding of Hemokinin 1, unlocking its full potential as a therapeutic target.
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