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Proteintech anti hcn2
Anti Hcn2, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti hcn2 - by Bioz Stars, 2026-10
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Incubation:

Article Title: HCN channels in the lateral habenula regulate pain and comorbid depressive‐like behaviors in mice
Article Snippet: All sections were rinsed using PBS and incubated in a blocking solution containing 0.3% Trion X‐100 (X‐100, Sigma, USA), 1% bovine serum albumin (A4503, Sigma, USA), and 1% normal donkey serum (ab7475, Sigma, USA). .. Subsequently, the sections were incubated with primary antibodies including anti‐HCN1 (55222‐1‐AP, 1:200, rabbit, Proteintech, USA), anti‐HCN2 (55245‐1‐AP, 1:200, rabbit, Proteintech, USA), anti‐HCN3 (APC‐057, 1:200, rabbit, Alomone Labs, Israel), anti‐HCN4 (APC‐052, 1:200, rabbit, Alomone Labs, Israel), anti‐NeuN (26004, 1:200, Guinea pig, Synaptic Systems, Germany), anti‐GFAP (ab53554, 1:400, Goat, Abcam, UK), anti‐Iba1 (011‐27991, 1:200, Goat, Wako, Japan), and anti‐c‐FOS (2250S, 1:1000, Rabbit, Cell Signaling Technology, USA) for 3 days at 4°C. .. Subsequently, the sections were rinsed with PBS three times and incubated with the appropriate secondary antibodies, namely, Alexa Fluor 555 (A31572, 1: 400, Rabbit, Invitrogen, USA), Alexa Fluor 555 (A21432, 1: 400, Goat, Invitrogen, USA), Alexa Fluor 647 (A31573, 1: 400, Rabbit, Invitrogen, USA), or Cy5 (706‐175‐148, 1:400, guinea pig, Jackson ImmunoResearch, USA) for 1 h at room temperature.

Article Title: Thalamocortical Circuit Controls Neuropathic Pain via Up-regulation of HCN2 in the Ventral Posterolateral Thalamus
Article Snippet: .. Subsequently, the membrane was blocked at room temperature for 1 h and incubated with rabbit polyclonal anti-HCN1 (1:1000; Proteintech, IL, USA) and anti-HCN2 (1:1000; Proteintech) or rabbit polyclonal anti-β-actin (1:1000; Proteintech) antibodies at 4 °C overnight. .. After 3 washes, the membranes were incubated with goat anti-rabbit IgG secondary antibody (1:2000; Thermo Fisher Scientific, MA, USA) for 2 h at room temperature.

Article Title: HCN2 contributes to oxaliplatin-induced neuropathic pain through activation of the CaMKII/CREB cascade in spinal neurons
Article Snippet: .. The membranes were placed in the block buffer at room temperature for 1 h and incubated with one of the following primary antibodies: anti-HCN2 (Proteintech, Wuhan, China), anti-NR2B (Proteintech), anti-pCaMKII (Cell Signalling Technology, USA); anti-CaMKII (Cell Signalling Technology); anti-pCREB (Cell Signalling Technology); anti-CREB (Cell Signalling Technology) at 4°C for 12 h, and then incubated with horseradish peroxidase-conjugated anti-rabbit IgG (Proteintech) for 1 h. Quantification of the band for each protein was performed with Image J software. .. Total RNA was isolated using the TRIzol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer’s protocol.

Article Title: HCN2 contributes to oxaliplatin-induced neuropathic pain by inducing spinal long-term potentiation via activation of NMDA receptor-mediated CaMKII signaling.
Article Snippet: Our previous findings indicate that HCN2 contributes to oxaliplatin-induced neuropathic pain, but the mechanisms underlying the development of neuropathic pain are still unclear.. Here, we found that the rat HCN2 levels significantly increased after high-frequency stimulation–induced long-term potentiation (LTP).. Spinal local application of ZD7288 (a cyclic-nucleotide-gated-channel–specific inhibitor) prevented LTP induction after intraperitoneal injection of oxaliplatin.

Cell-Signaling:

Article Title: HCN channels in the lateral habenula regulate pain and comorbid depressive‐like behaviors in mice
Article Snippet: All sections were rinsed using PBS and incubated in a blocking solution containing 0.3% Trion X‐100 (X‐100, Sigma, USA), 1% bovine serum albumin (A4503, Sigma, USA), and 1% normal donkey serum (ab7475, Sigma, USA). .. Subsequently, the sections were incubated with primary antibodies including anti‐HCN1 (55222‐1‐AP, 1:200, rabbit, Proteintech, USA), anti‐HCN2 (55245‐1‐AP, 1:200, rabbit, Proteintech, USA), anti‐HCN3 (APC‐057, 1:200, rabbit, Alomone Labs, Israel), anti‐HCN4 (APC‐052, 1:200, rabbit, Alomone Labs, Israel), anti‐NeuN (26004, 1:200, Guinea pig, Synaptic Systems, Germany), anti‐GFAP (ab53554, 1:400, Goat, Abcam, UK), anti‐Iba1 (011‐27991, 1:200, Goat, Wako, Japan), and anti‐c‐FOS (2250S, 1:1000, Rabbit, Cell Signaling Technology, USA) for 3 days at 4°C. .. Subsequently, the sections were rinsed with PBS three times and incubated with the appropriate secondary antibodies, namely, Alexa Fluor 555 (A31572, 1: 400, Rabbit, Invitrogen, USA), Alexa Fluor 555 (A21432, 1: 400, Goat, Invitrogen, USA), Alexa Fluor 647 (A31573, 1: 400, Rabbit, Invitrogen, USA), or Cy5 (706‐175‐148, 1:400, guinea pig, Jackson ImmunoResearch, USA) for 1 h at room temperature.

Blocking Assay:

Article Title: HCN-Channel-Dependent Hyperexcitability of the Layer V Pyramidal Neurons in IL-mPFC Contributes to Fentanyl-Induced Hyperalgesia in Male Rats.
Article Snippet: Then, brains were cryoprotected in 20% sucrose for 24 h at 4 °C followed by 30% sucrose for 24 h. Brain free-floating Sects. (30 μm) cut on vibration microtome (LEICA VT1200S) in chilled 0.1 M PBS were prepared for immunohistochemical staining. .. QuickBlockTM Blocking Buffer for Immunol Staining (Beyotime, Wuhan, China) was used to block the brain slices in a 24-well Tissue Culture Plate (Biofil, Guangzhou, China) for 10 min at room temperature, then incubating the Sects. (12–24 h at 4 °C) with the primary antibodies: anti c-Fos (1:300, rabbit, CST technology), anti-HCN1 (1:100, rabbit, Abclonal), anti-HCN2 (1:100, rabbit, Proteintech), and anti-CaMKIIα (1:300, mouse, CST). .. QuickBlockTM Primary Antibody Dilution Buffer for Immunol Staining (Beyotime, Wuhan, China) was used to dilute the primary antibodies.

Article Title: HCN2 contributes to oxaliplatin-induced neuropathic pain through activation of the CaMKII/CREB cascade in spinal neurons
Article Snippet: .. The membranes were placed in the block buffer at room temperature for 1 h and incubated with one of the following primary antibodies: anti-HCN2 (Proteintech, Wuhan, China), anti-NR2B (Proteintech), anti-pCaMKII (Cell Signalling Technology, USA); anti-CaMKII (Cell Signalling Technology); anti-pCREB (Cell Signalling Technology); anti-CREB (Cell Signalling Technology) at 4°C for 12 h, and then incubated with horseradish peroxidase-conjugated anti-rabbit IgG (Proteintech) for 1 h. Quantification of the band for each protein was performed with Image J software. .. Total RNA was isolated using the TRIzol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer’s protocol.

Staining:

Article Title: HCN-Channel-Dependent Hyperexcitability of the Layer V Pyramidal Neurons in IL-mPFC Contributes to Fentanyl-Induced Hyperalgesia in Male Rats.
Article Snippet: Then, brains were cryoprotected in 20% sucrose for 24 h at 4 °C followed by 30% sucrose for 24 h. Brain free-floating Sects. (30 μm) cut on vibration microtome (LEICA VT1200S) in chilled 0.1 M PBS were prepared for immunohistochemical staining. .. QuickBlockTM Blocking Buffer for Immunol Staining (Beyotime, Wuhan, China) was used to block the brain slices in a 24-well Tissue Culture Plate (Biofil, Guangzhou, China) for 10 min at room temperature, then incubating the Sects. (12–24 h at 4 °C) with the primary antibodies: anti c-Fos (1:300, rabbit, CST technology), anti-HCN1 (1:100, rabbit, Abclonal), anti-HCN2 (1:100, rabbit, Proteintech), and anti-CaMKIIα (1:300, mouse, CST). .. QuickBlockTM Primary Antibody Dilution Buffer for Immunol Staining (Beyotime, Wuhan, China) was used to dilute the primary antibodies.

Membrane:

Article Title: Thalamocortical Circuit Controls Neuropathic Pain via Up-regulation of HCN2 in the Ventral Posterolateral Thalamus
Article Snippet: .. Subsequently, the membrane was blocked at room temperature for 1 h and incubated with rabbit polyclonal anti-HCN1 (1:1000; Proteintech, IL, USA) and anti-HCN2 (1:1000; Proteintech) or rabbit polyclonal anti-β-actin (1:1000; Proteintech) antibodies at 4 °C overnight. .. After 3 washes, the membranes were incubated with goat anti-rabbit IgG secondary antibody (1:2000; Thermo Fisher Scientific, MA, USA) for 2 h at room temperature.

Article Title: HCN2 contributes to oxaliplatin-induced neuropathic pain by inducing spinal long-term potentiation via activation of NMDA receptor-mediated CaMKII signaling.
Article Snippet: Our previous findings indicate that HCN2 contributes to oxaliplatin-induced neuropathic pain, but the mechanisms underlying the development of neuropathic pain are still unclear.. Here, we found that the rat HCN2 levels significantly increased after high-frequency stimulation–induced long-term potentiation (LTP).. Spinal local application of ZD7288 (a cyclic-nucleotide-gated-channel–specific inhibitor) prevented LTP induction after intraperitoneal injection of oxaliplatin.

Software:

Article Title: HCN2 contributes to oxaliplatin-induced neuropathic pain through activation of the CaMKII/CREB cascade in spinal neurons
Article Snippet: .. The membranes were placed in the block buffer at room temperature for 1 h and incubated with one of the following primary antibodies: anti-HCN2 (Proteintech, Wuhan, China), anti-NR2B (Proteintech), anti-pCaMKII (Cell Signalling Technology, USA); anti-CaMKII (Cell Signalling Technology); anti-pCREB (Cell Signalling Technology); anti-CREB (Cell Signalling Technology) at 4°C for 12 h, and then incubated with horseradish peroxidase-conjugated anti-rabbit IgG (Proteintech) for 1 h. Quantification of the band for each protein was performed with Image J software. .. Total RNA was isolated using the TRIzol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer’s protocol.

Transfection:

Article Title: Non-CpG methylation by DNMT3B facilitates REST binding and gene silencing in developing mouse hearts
Article Snippet: .. Primary embryonic and neonatal ventricular cardiomyocytes were seeded onto Matrigel-coated Nunc Thermanox and poly-L-lysine/laminin-coated glass coverslips, transfected with 100 nM siRNA for Dnmt3a, Dnmt3b or Rest by the Lipofectamine LTX and PLUS Reagents for 48 h, and then exposed to anti-HCN2 (Proteintech, 555245-1-AP, 1:500), REST (Antibodies-online, ABIN747683, 1:500) and DNMT3B (Abcam, ab13604, 1:500) antibodies. ..



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HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and <t>HCN2</t> (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.
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HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and <t>HCN2</t> (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.
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HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and <t>HCN2</t> (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.
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HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and <t>HCN2</t> (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.
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HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and <t>HCN2</t> (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.
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Image Search Results


HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and HCN2 (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.

Journal: The Journal of Comparative Neurology

Article Title: Distribution of Voltage‐Gated Sodium Channels and Scaffolding Proteins on Vestibular Calyx Ending Delineates the Axon Initial Segment

doi: 10.1002/cne.70127

Figure Lengend Snippet: HCN, an I h ion channel, localized to both inner and outer surfaces of calyces. (A) Section from the CZ of a female rat crista immunolabeled for calretinin ( Calret , green ) and HCN2 (red) in several calretinin‐positive calyx‐only afferents; a single calretinin‐negative dimorphic calyx ( D ) is present. In (A’), the calretinin label seen in (A) has been removed to show light HCN2 labeling of all calyces, including the dimorphic calyx ending. (B, B’) Same immunolabeling as in (A, A’), but from the PZ. A single type II hair cell ( II ) and several dimorphic ( D ) calyces are present; the calyces are slightly more heavily labeled for HCN2 than are those in the CZ; the type II hair cell is very lightly HCN2 labeled. HCN2 label is found on both the inner and outer surfaces of the calyx ( arrows ). Scale bar (for all four panels) = 5 µm.

Article Snippet: HCN2 , NeuroMab , 75‐111 RRID:AB_2279449 , , , , , , Datasheet.

Techniques: Immunolabeling, Labeling