LINE IMMUNOASSAY FOR CONFIRMATION AND DISCRIMINATION OF HUMAN T-CELL LYMPHOTROPIC VIRUS INFECTIONS IN INCONCLUSIVE WESTERNBLOT SERUM SAMPLES FROM BRAZIL.
Difficulties to substantiate and discriminate human T-cell lymphotropic virus sorts 1 and a pair of (HTLV-1 and HTLV-2) infections by serological Western Blotting (WB) assay (HTLV Blot 2.4, MP Biomedicals) has been reported in Brazil, primarily in HIV/AIDS sufferers, with numerous WB-indeterminate and WB-positive however HTLV untypeable outcomes.
Nonetheless, the line immunoassay (LIA) (INNO-LIA HTLV-I/II, Fujirebio) was pointed to improve specificity and sensitivity for confirming HTLV-1\/2 infections. So as to add info in regards to the improved skill of LIA in relation to WB when utilized in samples of people from totally different risk-groups from Brazil, we carried out the current examine.
Three teams have been analyzed: group 1 [G1], 62 samples from HIV/AIDS sufferers from São Paulo-SP (48 WB-indeterminate + 14 HTLV); group 2 [G2], 24 samples from sufferers with hepatitis B or hepatitis C from São Paulo (21 WB-indeterminate + Three HTLV; 17 HIV-seropositive), and group 3 [G3], 25 samples from HTLV out-patients clinic from Salvador-Bahia (16 WB-indeterminate + 9 HTLV; all HIV-seronegative).
General, the LIA confirmed HTLV-1\/2 an infection (HTLV-1, HTLV-2 or HTLV) in 66.1% [G1], 83.3% [G2], and 76.0% [G3] of samples. Curiously, nearly all of WB-indeterminate outcomes have been confirmed by LIA as HTLV-2 in G1 and G2, however not in G3, wherein the samples have been outlined as HTLV-1 or HTLV positives. These outcomes agree with the virus sorts that flow into in such sufferers of various areas in Brazil, and emphasize the LIA as the very best serological take a look at for confirming HTLV-1 and HTLV-2 infections, independently of being utilized in HTLV-monoinfected or HTLV-coinfected people.
Description: A sandwich quantitative ELISA assay kit for detection of Human Kelch Like ECH Associated Protein 1 (KEAP1) in samples from serum, plasma, tissue homogenates or other biological fluids.
Human Kelch Like ECH Associated Protein 1 (KEAP1) ELISA Kit
Description: A sandwich quantitative ELISA assay kit for detection of Human Kelch Like ECH Associated Protein 1 (KEAP1) in samples from serum, plasma, tissue homogenates or other biological fluids.
Mouse Kelch Like ECH Associated Protein 1 (KEAP1) ELISA Kit
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Kelch Like ECH Associated Protein 1 (KEAP1) in samples from serum, plasma, tissue homogenates or other biological fluids.
Mouse Kelch Like ECH Associated Protein 1 (KEAP1) ELISA Kit
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Kelch Like ECH Associated Protein 1 (KEAP1) in samples from serum, plasma, tissue homogenates or other biological fluids.
Rat Kelch Like ECH Associated Protein 1 (KEAP1) ELISA Kit
Description: A sandwich quantitative ELISA assay kit for detection of Rat Kelch Like ECH Associated Protein 1 (KEAP1) in samples from serum, plasma, tissue homogenates or other biological fluids.
Rat Kelch Like ECH Associated Protein 1 (KEAP1) ELISA Kit
Description: A sandwich quantitative ELISA assay kit for detection of Rat Kelch Like ECH Associated Protein 1 (KEAP1) in samples from serum, plasma, tissue homogenates or other biological fluids.
Human Kelch Like ECH Associated Protein 1 (KEAP1) ELISA Kit
Description: KEAP1 Antibody: KEAP1 (kelch-like ECH-associated protein 1) is a stress sensing adaptor for the Cullin3 (Cul3)-dependent E3 ubiquitin ligase complex that negatively regulates NRF2 (NF-E2-related factor 2) and plays a role in the oxidative stress response. It targets NFE2L2/NRF2 for ubiquitination and degradation by the proteasome. KEAP1 contains an amino terminal BTB/POZ domain and a carboxyl terminal KELCH domain which are required for interaction with NRF2, and in binding Cul3-E3 ubiquitin ligase. Altered expression of NRF2 is associated with chronic obstructive pulmonary disease (COPD). KEAP1 also targets the down regulation of NF-κB activity by targeting IKKβ degradation. Mutation of the KEAP1 gene is found in lung cancer.
Description: KEAP1 Antibody: KEAP1 (kelch-like ECH-associated protein 1) is a stress sensing adaptor for the Cullin3 (Cul3)-dependent E3 ubiquitin ligase complex that negatively regulates NRF2 (NF-E2-related factor 2) and plays a role in the oxidative stress response. It targets NFE2L2/NRF2 for ubiquitination and degradation by the proteasome. KEAP1 contains an amino terminal BTB/POZ domain and a carboxyl terminal KELCH domain which are required for interaction with NRF2, and in binding Cul3-E3 ubiquitin ligase. Altered expression of NRF2 is associated with chronic obstructive pulmonary disease (COPD). KEAP1 also targets the down regulation of NF-κB activity by targeting IKKβ degradation. Mutation of the KEAP1 gene is found in lung cancer.
Description: A polyclonal antibody against KEAP1. Recognizes KEAP1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:2000-1:5000, IHC:1:25-1:100
Description: A polyclonal antibody against KEAP1. Recognizes KEAP1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/20000
Description: A polyclonal antibody against KEAP1. Recognizes KEAP1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:2000-1:5000, IHC:1:25-1:100
Description: A polyclonal antibody against KEAP1. Recognizes KEAP1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC
Description: A polyclonal antibody against KEAP1. Recognizes KEAP1 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC; Recommended dilution: WB:1:200-1:1000, IHC:1:20-1:200
Description: A polyclonal antibody against Keap1. Recognizes Keap1 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, WB; Recommended dilution: WB:1:500-1:2000
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.
Description: Description of target: This gene encodes a protein containing KELCH-1 like domains, as well as a BTB/POZ domain. Kelch-like ECH-associated protein 1 interacts with NF-E2-related factor 2 in a redox-sensitive manner and the dissociation of the proteins in the cytoplasm is followed by transportation of NF-E2-related factor 2 to the nucleus. This interaction results in the expression of the catalytic subunit of gamma-glutamylcysteine synthetase. Two alternatively spliced transcript variants encoding the same isoform have been found for this gene.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 40.6pg/mL
Description: Description of target: Acts as a substrate adapter protein for the E3 ubiquitin ligase complex formed by CUL3 and RBX1 and targets NFE2L2/NRF2 for ubiquitination and degradation by the proteasome, thus resulting in the suppression of its transcriptional activity and the repression of antioxidant response element-mediated detoxifying enzyme gene expression. Retains NFE2L2/NRF2 and may also retain BPTF in the cytosol. Targets PGAM5 for ubiquitination and degradation by the proteasome.<p>This subsection of the <a href="//www.uniprot.org/help/function_section">‘Function’</a> section describes the metabolic pathway(s) associated with a protein.<p><a href='/help/pathway' target='_top'>More...</a></p>Pathwayi: protein ubiquitinationThis protein is involved in the pathway protein ubiquitination, which is part of Protein modification._x000D_View all proteins of this organism that are known to be involved in the pathway protein ubiquitination and in Protein modification. ;Species reactivity: Rat;Application: ;Assay info: Assay Methodology: Quantitative Sanadwich ELISA;Sensitivity: 11.75 pg/mL
Description: Description of target: Acts as a substrate adapter protein for the E3 ubiquitin ligase complex formed by CUL3 and RBX1 and targets NFE2L2/NRF2 for ubiquitination and degradation by the proteasome, thus resulting in the suppression of its transcriptional activity and the repression of antioxidant response element-mediated detoxifying enzyme gene expression. Retains NFE2L2/NRF2 and may also retain BPTF in the cytosol. Targets PGAM5 for ubiquitination and degradation by the proteasome.5 Publications
<p>Manually curated information for which there is published experimental evidence.</p>
<p><a href="/manual/evidences#ECO:0000269">More…</a></p> Manual assertion based on experiment iniRef.7"Distinct cysteine residues in Keap1 are required for Keap1-dependent ubiquitination of Nrf2 and for stabilization of Nrf2 by chemopreventive agents and oxidative stress."_x005F_x005F_x000D_Zhang D.D., Hannink M._x005F_x005F_x000D_Mol. Cell. Biol. 23:8137-8151(2003) [PubMed] [Europe PMC] [Abstract]Cited for: FUNCTION, MUTAGENESIS OF CYS-151; CYS-273 AND CYS-288, SUBCELLULAR LOCATION.Ref.8"Fetal Alz-50 clone 1 interacts with the human orthologue of the Kelch-like Ech-associated protein."_x005F_x005F_x000D_Strachan G.D., Morgan K.L., Otis L.L., Caltagarone J., Gittis A., Bowser R., Jordan-Sciutto K.L._x005F_x005F_x000D_Biochemistry 43:12113-12122(2004) [PubMed] [Europe PMC] [Abstract]Cited for: INTERACTION WITH NF2L2/NRF2 AND BPTF, FUNCTION, TISSUE SPECIFICITY, SUBCELLULAR LOCATION.Ref.9"Keap1 is a redox-regulated substrate adaptor protein for a Cul3-dependent ubiquitin ligase complex."_x005F_x005F_x000D_Zhang D.D., Lo S.-C., Cross J.V., Templeton D.J., Hannink M._x005F_x005F_x000D_Mol. Cell. Biol. 24:10941-10953(2004) [PubMed] [Europe PMC] [Abstract]Cited for: FUNCTION, INTERACTION WITH CUL3 AND RBX1, MUTAGENESIS OF 125-ILE--GLY-127 AND 162-TYR--ILE-164, UBIQUITINATION.Ref.10"Ubiquitination of Keap1, a BTB-Kelch substrate adaptor protein for Cul3, targets Keap1 for degradation by a proteasome-independent pathway."_x005F_x005F_x000D_Zhang D.D., Lo S.C., Sun Z., Habib G.M., Lieberman M.W., Hannink M._x005F_x005F_x000D_J. Biol. Chem. 280:30091-30099(2005) [PubMed] [Europe PMC] [Abstract]Cited for: FUNCTION, IDENTIFICATION IN A COMPLEX WITH CUL3 AND RBX1, UBIQUITINATION, ENZYME REGULATION, MUTAGENESIS OF CYS-151.Ref.13"PGAM5, a Bcl-XL-interacting protein, is a novel substrate for the redox-regulated Keap1-dependent ubiquitin ligase complex."_x005F_x005F_x000D_Lo S.-C., Hannink M._x005F_x005F_x000D_J. Biol. Chem. 281:37893-37903(2006) [PubMed] [Europe PMC] [Abstract]Cited for: INTERACTION WITH PGAM5, FUNCTION, ENZYME REGULATION, DOMAIN, MUTAGENESIS OF CYS-151; TYR-334; ARG-415; ARG-483 AND TYR-572. ;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich Immunoassay;Sensitivity: < 0.056 ng/mL
Description: Description of target: Acts as a substrate adapter protein for the E3 ubiquitin ligase complex formed by CUL3 and RBX1 and targets NFE2L2/NRF2 for ubiquitination and degradation by the proteasome, thus resulting in the suppression of its transcriptional activity and the repression of antioxidant response element-mediated detoxifying enzyme gene expression. Retains NFE2L2/NRF2 and may also retain BPTF in the cytosol. Targets PGAM5 for ubiquitination and degradation by the proteasome (By similarity).By similarity2 Publications
<p>Manually curated information for which there is published experimental evidence.</p>
<p><a href="/manual/evidences#ECO:0000269">More…</a></p> Manual assertion based on experiment iniRef.1"Keap1 represses nuclear activation of antioxidant responsive elements by Nrf2 through binding to the amino-terminal Neh2 domain."_x005F_x005F_x000D_Itoh K., Wakabayashi N., Katoh Y., Ishii T., Igarashi K., Engel J.D., Yamamoto M._x005F_x005F_x000D_Genes Dev. 13:76-86(1999) [PubMed] [Europe PMC] [Abstract]Cited for: NUCLEOTIDE SEQUENCE [MRNA], FUNCTION.Ref.6"Keap1-dependent proteasomal degradation of transcription factor Nrf2 contributes to the negative regulation of antioxidant response element-driven gene expression."_x005F_x005F_x000D_McMahon M., Itoh K., Yamamoto M., Hayes J.D._x005F_x005F_x000D_J. Biol. Chem. 278:21592-21600(2003) [PubMed] [Europe PMC] [Abstract]Cited for: FUNCTION. <p>Describes the metabolic pathway(s) associated with a protein.</p><p><a href='../manual/pathway' target='_top'>More...</a></p>Pathwayi: protein ubiquitinationThis protein is involved in the pathway protein ubiquitination, which is part of Protein modification._x005F_x005F_x000D_View all proteins of this organism that are known to be involved in the pathway protein ubiquitination and in Protein modification. ;Species reactivity: Mouse;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich Immunoassay;Sensitivity: < 0.055 ng/mL
Description: A polyclonal antibody for detection of Keap1 from Human, Mouse, Rat. This Keap1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human Keap1
Description: A polyclonal antibody for detection of Keap1 from Human, Mouse, Rat. This Keap1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human Keap1
Description: A polyclonal antibody for detection of Keap1 from Human, Mouse, Rat. This Keap1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human Keap1
Fuzhisan ameliorates Aβ manufacturing and tau phosphorylation in hippocampal of 11month previous APP/PS1 transgenic mice: A Westernblot examine.
Accumulation of amyloid-β (Aβ) peptide and deposition of hyperphosphorylated tau protein are two main pathological hallmarks of Alzheimer’s illness (AD). Glycogen synthase kinase-3β (GSK3β) is more and more thought to play a pivotal function within the pathogenesis of AD, each as a regulator of the manufacturing of Aβ and thru its well-established function on tau phosphorylation.
The phosphoinositide Three kinase (PI3K)/Akt pathway performs an import function in neuronal survival and cognitive operate, and is called an upstream component of GSK3β. Fuzhisan (FZS), a Chinese language natural complicated prescription, has been used for the therapy of AD for over 20years, and is understood to boost the cognitive skill in AD sufferers in addition to in AD mannequin rats.
Nonetheless, it nonetheless stays unclear whether or not FZS is accountable for regulation of PI3K/AKT/GSK3β signaling and contributes to subsequent down-regulation of Aβ and phosphorylated tau. Thus, we handled APP/PS1 transgenic mice, a helpful mannequin of AD-related reminiscence impairment, with FZS by intragastrical administration for 60days and Donepezil was used as a constructive management.
The outcomes confirmed that therapy with FZS considerably reversed the reminiscence deficit within the Tg APP/PS1 mice within the Morris water maze take a look at. Furthermore, FZS considerably attenuated Aβ manufacturing by means of inhibition of APP procession and phosphorylation of tau within the hippocampus of Tg APP/PS1 mice.
As well as, FZS therapy additionally elevated PI3K and pSer473-AKT ranges, inhibited GSK3β exercise by rising phosphorylation of GSK3β at Ser9. These outcomes indicated that the reminiscence ameliorating impact of FZS could also be, partially, by regulation the PI3K/AKT/GSK3β signaling which can contribute to down-regulation of Aβ and tau hyperphosphorylation.
A Hypoglycemia-inducing Large Borderline Phyllodes Tumor Secreting Excessive-molecular-weight Insulin-Like Progress Issue II: A Case Report with Immunohistochemistry and a WesternBlot Evaluation.
A 50-year-old lady with a big proper breast mass was emergently hospitalized for generalized weak spot and fatigue. A histological examination of tumor biopsy specimens revealed a phyllodes tumor (PT). She all of the sudden misplaced consciousness as a result of extreme hypoglycemia.
Non-islet cell tumor hypoglycemia (NICTH) because of the PT was suspected. The tumor was emergently resected. A histological examination revealed a borderline PT. The affected person recovered from the hypoglycemic episode. Excessive-molecular-weight insulin-like development issue II was detected in serum that had been collected preoperatively and within the tumor tissue, however not in serum that had been collected postoperatively. We herein current a case of a borderline PT with NICTH.
Immunohistochemical and westernblot evaluation counsel that the soluble types of FGF1-2 and FGFR1-2 maintain tail regeneration within the lizard.
Fibroblast Progress Components 1-2 (FGF1-2) stimulate tail regeneration in lizards and due to this fact the distribution of their receptors, FGFR1-2, within the regenerating tail of the lizard. Podarcis muralis has been studied utilizing immunofluorescence and western blotting. Immunoreactive protein bands at 15-16kDa for FGF1-2 along with these at 50-65kDa are detected within the regenerating dermis, however weak bands at 35, 45 and 50kDa seem from the regenerating connective tissues.
Strongly immunolabeled bands for FGFR1 at 32, 60, and 80kDa and fewer intense for FGFR2 solely seem within the regenerating tail. In regular tail dermis and dermis, greater MW kinds are current at 80 and 115-140kDa, respectively, however they disappear within the regenerating dermis and dermis the place low MW types of FGFR1-2 are discovered at 50-70kDa.
Immunolocalization confirms that the majority FGFR1-2 are current within the wound dermis, Apical Epidermal Peg, ependymal tube whereas immunolabeling lowers in regenerating muscle mass, blastema cells, cartilage and connectives tissues. The seemingly launch of FGFs from the Apical Epidermal Peg and ependyma and the presence of their receptors in these tissues might decide the autocrine stimulation of proliferation and a paracrine stimulation of the blastema cells by means of their FGF Receptors.
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.
Description: Western blot detection of IP proteins can exhibit high background due to the use of the same primary antibody in the IP and the Western blot. The Pure-IP Western Blot Detection Kit eliminates this background problem by using a proprietary HRP Conjugate for detection of the primary antibody.
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.
Box Western Blot Polystyrene Transparent 95x30x16mm X5
Description: The human tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 9 different human normal tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane. The human normal tissues included in the blot are brain, heart, kidney, liver, lung, pancreas, skeletal muscle, skin, and spleen.
Description: The human tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 9 different human normal tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane.The human normal tissues included in the blot are left cerebellum, right cerebellum, frontal lobe, occipital lobe, parietal lobe, whole eye, spinal cord, temporal lobe, and thalamus.
Description: The human tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 9 different human tumor tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane. The human tumor tissues included in the blot are brain, colon, kidney, liver, lung, pancreas, skin, spleen, and stomach.
Description: The human tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different human tumor tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane.The human tumor tissues included in the blot are colon, duodenum, esophagus, small intestine, liver, pancreas, rectum, and stomach.
Description: The human tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different human tumor tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane.The human tumor tissues included in the blot are bladder, breast, kidney, ovary, prostate, testis, cervix, and uterus.
Description: The human tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different human tumor tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane. The human tumor tissues included in the blot are kidney, liver, lymphoma, Non-Hodgkin's lymphoma, spleen, thymoma, thyroid, and tonsil.
Description: The mouse tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different mouse tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane. The mouse tissues included in the blot are brain, colon, heart, kidney, liver, lung, pancreas, and spleen.
Description: The mouse tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different mouse tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane.The mouse tissues included in the blot are adrenal, cerebellum, cerebrum, small intestine, skeletal muscle, stomach, testis, and thymus.
Description: The rat tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different rat tissue lysates with 15 µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane.The rat tissues included in the blot are brain, colon, heart, kidney, liver, lung, pancreas, and spleen.
Description: The rat tissue blot is designed for proteomics research in screening for antibody and protein expression. It carries 8 different rat tissue lysates with 15µg of total cellular protein in each lane. Proteins were separated in 4-20% SDS-PAGE gel and transferred onto nitrocellulose membrane. The rat tissues included in the blot are adrenal, cerebellum, cerebrum, small intestine, skeletal muscle, stomach, testis, and thymus.
Description: This substrate is ideal for quick, sensitive chemiluminescent detection of horseradish peroxidase (HRP). It’s particularly useful for detecting HRP-labeled secondary antibodies or streptavidin-HRP in immunoblotting applications.
Custom Assortment of EPOXIED Assemblies - 20 total Mount/Base assemblies
Custom Contents Listed Below
([Qty of Pin/base]x B-[mount style]-[aperture size]-[base style])
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