Expression of Escherichia coli araE and modified lacYgenes in Campylobacter jejuni will not be enough for arabinose transport
Introduction: Not like Escherichia coli , Campylobacter jejuni is unable to import a variety of sugars, together with arabinose, which makes frequent expression vectors, comparable to pBAD33, non-functional in these micro organism.
Purpose: The intention of this research was to research whether or not the E. coli transporters AraE and modified LacY (LacYA177C) would allow C. jejuni to uptake arabinose.
Methodology and outcomes: The respective genes of E. coli have been constitutively expressed in C. jejuni pressure 11168H after integration into the chromosome through homologous recombination. Vectors carrying these genes additionally contained a reporter gene, gfp, beneath the management of the arabinose-inducible promoter, pBAD. These constructs have been verified in E. coli by demonstrating the induction of gfp within the presence of arabinose. Integration of the genes into one of many rRNA gene clusters was verified by PCR and genome sequencing.
The latter additionally confirmed that the inserted gene clusters contained no mutations. Expression of the gfp gene within the presence of arabinose inducer was monitored utilizing fluorescence microscopy of colonies and fluorimetry utilizing each entire cells and lysates.
Conclusion: The outcomes demonstrated the lack of C. jejuni to make use of arabinose transporters, that are totally purposeful in E. coli , suggesting a outstanding distinction within the physiology of those micro organism.
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human NR6A1 / GCNF (Ligand-binding Domain). This antibody is tested and proven to work in the following applications:
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined.
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene.
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]
Description: A polyclonal antibody for alpha Tubulin from Human. The antibody is produced in rabbit after immunization with human synthetic peptide of Human alpha-Tubulin. The Antibody is tested and validated for WB, ICC/IF assays with the following recommended dilutions: WB (1:1000); ICC/IF (1:100). This alpha Tubulin antibody is unconjugated.
Description: A polyclonal antibody for alpha Tubulin from Human. The antibody is produced in rabbit after immunization with human synthetic peptide of Human alpha-Tubulin. The Antibody is tested and validated for WB, ICC/IF assays with the following recommended dilutions: WB (1:1000); ICC/IF (1:100). This alpha Tubulin antibody is conjugated to ATTO 390.
Description: A polyclonal antibody for alpha Tubulin from Human. The antibody is produced in rabbit after immunization with human synthetic peptide of Human alpha-Tubulin. The Antibody is tested and validated for WB, ICC/IF assays with the following recommended dilutions: WB (1:1000); ICC/IF (1:100). This alpha Tubulin antibody is conjugated to ATTO 488.
Description: A polyclonal antibody for alpha Tubulin from Human. The antibody is produced in rabbit after immunization with human synthetic peptide of Human alpha-Tubulin. The Antibody is tested and validated for WB, ICC/IF assays with the following recommended dilutions: WB (1:1000); ICC/IF (1:100). This alpha Tubulin antibody is conjugated to ATTO 565.
Description: A polyclonal antibody for alpha Tubulin from Human. The antibody is produced in rabbit after immunization with human synthetic peptide of Human alpha-Tubulin. The Antibody is tested and validated for WB, ICC/IF assays with the following recommended dilutions: WB (1:1000); ICC/IF (1:100). This alpha Tubulin antibody is conjugated to ATTO 594.
Description: A polyclonal antibody for alpha Tubulin from Human. The antibody is produced in rabbit after immunization with human synthetic peptide of Human alpha-Tubulin. The Antibody is tested and validated for WB, ICC/IF assays with the following recommended dilutions: WB (1:1000); ICC/IF (1:100). This alpha Tubulin antibody is conjugated to ATTO 633.
Genome-Huge Evaluation of Peptidoglycan Recognition Protein Genes in Fig Wasps (Hymenoptera, Chalcidoidea)
The innate immunity is a very powerful protection in opposition to pathogen of bugs, and the peptidoglycan recognition proteins (PGRPs) play an essential function within the processes of immune recognition and initiation of Toll, IMD and different sign pathways.
In fig wasps, pollinators and non-pollinators current completely different evolutionary histories and existence, though each are carefully related to fig syconia, which can point out their completely different patterns within the evolution of PGRPs.
By handbook annotation, we bought all of the PGRP genes of 12 fig wasp species, containing seven pollinators and 5 non-pollinators, and investigated their putative completely different evolutionary patterns.
We discovered that the variety of PGRP genes in pollinators was considerably decrease than in non-pollinators, and the variety of catalytic PGRP introduced a declining pattern in pollinators.
Extra importantly, PGRP-SA is related to initiating the Toll pathway, in addition to gram-negative bacteria-binding proteins (GNBPs), which have been fully misplaced in pollinators, which led us to invest that the initiation of Toll pathway was less complicated in pollinators than in non-pollinators.
We concluded that fig pollinators owned a extra streamlined innate immune recognition system than non-pollinators. Our outcomes present molecular proof for the adaptive evolution of innate immunity in bugs of host specificity.
Comparative genomics of Alexander Fleming’s authentic Penicillium isolate (IMI 15378) reveals sequence divergence of penicillin synthesis genes
Antibiotics have been derived initially from wild organisms and due to this fact understanding how these compounds evolve amongst completely different lineages would possibly assist with the design of recent antimicrobial medicine. We report the draft genome sequence of Alexander Fleming’s authentic fungal isolate behind the invention of penicillin, now labeled as Penicillium rubens Biourge (1923) (IMI 15378). We examine the construction of the genome and genes concerned in penicillin synthesis with these in two ‘excessive producing’ industrial strains of P. rubens and the carefully associated species P. nalgiovense.
The primary effector genes for producing penicillin G (pcbAB, pcbC and penDE) present amino acid divergence between the Fleming pressure and each industrial strains, whereas a set of regulatory genes are conserved. Homologs of penicillin N effector genes cefD1 and cefD2 have been additionally discovered and the latter displayed amino acid divergence between the Fleming pressure and industrial strains.
The draft assemblies include a number of partial duplications of penicillin-pathway genes in all three P. rubens strains, to differing levels, which we hypothesise could be concerned in regulation of the pathway.
The 2 industrial strains are equivalent in sequence throughout all effector and regulatory genes however differ in duplication of the pcbAB-pcbC-penDE advanced and partial duplication of fragments of regulatory genes. We conclude that evolution within the wild encompassed each sequence adjustments of the effector genes and gene duplication, whereas human-mediated adjustments by mutagenesis and synthetic choice led to duplication of the penicillin pathway genes.
Description: This gene encodes a member of the alpha-actin binding protein gene family. The encoded protein is primarily expressed in skeletal muscle and functions as a structural component of sarcomeric Z line. This protein is involved in crosslinking actin containing thin filaments. An allelic polymorphism in this gene results in both coding and non-coding variants; the reference genome represents the coding allele. The non-functional allele of this gene is associated with elite athlete status.
Should the Human Actinin Alpha 3 (ACTN3) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human Actinin Alpha 3 (ACTN3) in samples from tissue homogenates, cell lysates or other biological fluids.
Should the Human Actinin Alpha 3 (ACTN3) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human Actinin Alpha 3 (ACTN3) in samples from tissue homogenates, cell lysates or other biological fluids.
Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IF, ELISA;WB:1/500-1/2000.IF:1/200-1/1000.ELISA:1/20000
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IF; Recommended dilution: IF:1:50-1:200
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, WB;ELISA:1:2000-1:5000, WB:1:500-1:2000
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, WB;ELISA:1:2000-1:5000, WB:1:500-1:2000
Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against ACTN2/ACTN3. Recognizes ACTN2/ACTN3 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, IF, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.IF:1/200-1/1000.ELISA:1/20000
Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
Description: A polyclonal antibody against ACTN2/ACTN3. Recognizes ACTN2/ACTN3 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC, IF;WB:1:500-1:3000, IHC:1:50-1:100, IF:1:100-1:500
Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
Description: A polyclonal antibody against ACTN2/ACTN3. Recognizes ACTN2/ACTN3 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC, IF;WB:1:500-1:3000, IHC:1:50-1:100, IF:1:100-1:500
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human ACTN3 . This antibody is tested and proven to work in the following applications:
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human. This antibody is HRP conjugated. Tested in the following application: ELISA
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human. This antibody is FITC conjugated. Tested in the following application: ELISA
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against ACTN3. Recognizes ACTN3 from Human. This antibody is Biotin conjugated. Tested in the following application: ELISA
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human ACTN3 (Center). This antibody is tested and proven to work in the following applications:
Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against ACTN1/ACTN2/ACTN3/ACTN4. Recognizes ACTN1/ACTN2/ACTN3/ACTN4 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.ELISA:1/20000
Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
Description: A polyclonal antibody against ACTN1/ACTN2/ACTN3/ACTN4. Recognizes ACTN1/ACTN2/ACTN3/ACTN4 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB;WB:1:500-1:3000
Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
Description: A polyclonal antibody against ACTN1/ACTN2/ACTN3/ACTN4. Recognizes ACTN1/ACTN2/ACTN3/ACTN4 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB;WB:1:500-1:3000
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human ACTN3 (aa1-50). This antibody is tested and proven to work in the following applications:
Description: Description of target: F-actin cross-linking protein which is thought to anchor actin to a variety of intracellular structures. This is a bundling protein.;Species reactivity: Mouse;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 41 pg/mL
Description: Description of target: This gene encodes a member of the alpha-actin binding protein gene family. The encoded protein is primarily expressed in skeletal muscle and functions as a structural component of sarcomeric Z line. This protein is involved in crosslinking actin containing thin filaments. An allelic polymorphism in this gene results in both coding and non-coding variants; the reference genome represents the coding allele. The non-functional allele of this gene is associated with elite athlete status.;Species reactivity: Human;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 4.1 pg/mL
Transposon Insertion within the purLGene Induces Biofilm Depletion in Escherichia coli ATCC 25922
Present Escherichia coli antibiofilm therapies comprise a mix of antibiotics generally used in opposition to planktonic cells, resulting in therapy failure. A greater understanding of the genes concerned in biofilm formation may facilitate the event of environment friendly and particular new antibiofilm therapies.
A complete of 2578 E. coli mutants have been generated by transposon insertion, of which 536 have been analysed on this research. After sequencing, Tn263 mutant, labeled as low biofilm-former (LF) in contrast to the wild-type (wt) pressure (ATCC 25922), confirmed an interruption within the purL gene, concerned within the de novo purine biosynthesis pathway.
To elucidate the function of purL in biofilm formation, a knockout was generated displaying decreased manufacturing of curli fibres, resulting in an impaired biofilm formation. These situations have been restored by complementation of the pressure or addition of exogenous inosine. Proteomic and transcriptional analyses have been carried out to characterise the variations attributable to purL alterations.
13 proteins have been altered in contrast to wt. The corresponding genes have been analysed by qRT-PCR not solely within the Tn263 and wt, but additionally in medical strains with completely different biofilm exercise. Total, this research means that purL is important for biofilm formation in E. coli and might be thought of as a possible antibiofilm goal.
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 Polyclonal Antibody (Human), Biotinylated)
 Polyclonal Antibody (Human), Cy3)
 Polyclonal Antibody (Human), FITC)
 Polyclonal Antibody (Human), HRP)
 Polyclonal Antibody (Human), PE)
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 Polyclonal Antibody (Human), APC-Cy7)
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Anti-ACTN3 antibody  ELISA Kit)
Human Actinin Alpha 3 (ACTN3) ELISA Kit 
Rabbit Polyclonal antibody Anti-CRBN )
Anti-ACTN3 Antibody (monoclonal, 9B5) 
ACTN3 Antibody 
ACTN3 antibody 
ACTN2/ACTN3 Antibody 
Polyclonal ACTN3 Antibody 
ACTN3 Conjugated Antibody 
ACTN2 / ACTN3 Antibody 
ACTN3 siRNA 
ACTN3 Antibody, HRP conjugated 
ACTN3 Antibody, FITC conjugated 
ACTN3 Antibody, Biotin conjugated )
Polyclonal ACTN3 Antibody (Center) 
Anti-Human ACTN3 DyLight® 488 conjugated Antibody 
Anti-Human ACTN3 DyLight® 550 conjugated Antibody 
Polyclonal Goat anti-GST α-form 
Polyclonal Goat anti-GST μ-form 
Polyclonal Goat anti-GST p-form 
ACTN3 Rabbit pAb 
ACTN3 Blocking Peptide 
ACTN1/ACTN2/ACTN3/ACTN4 Antibody  Antibody)
Actinin Alpha 3 (ACTN3) Antibody  Antibody)
Alpha Actinin 3 (ACTN3) Antibody )
Polyclonal ACTN3 Antibody (aa1-50) 
ACTN1 / ACTN2 / ACTN3 / ACTN4 Antibody 
Human ACTN3 ELISA Kit 
Goat ACTN3 ELISA Kit 
Canine ACTN3 ELISA Kit 
Anserini ACTN3 ELISA Kit 
Bovine ACTN3 ELISA Kit 
ACTN3 ELISA KIT|Human 
Human ACTN3 shRNA Plasmid 
Mouse ACTN3 shRNA Plasmid 
Mouse ACTN3 ELISA Kit 
Rat ACTN3 ELISA Kit 
Rabbit ACTN3 ELISA Kit 
Porcine ACTN3 ELISA Kit  Polyclonal Antibody (Human))
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human) 
Guinea Pig ACTN3 ELISA Kit  (pORF))
Actn3 ORF Vector (Rat) (pORF)  (pORF))
ACTN3 ORF Vector (Human) (pORF)  (pORF))
Actn3 ORF Vector (Mouse) (pORF) )
Recombinant Actinin Alpha 3 (ACTN3)  (OKEH05687))
ACTN3 ELISA Kit (Mouse) (OKEH05687)  (OKEH04449))
ACTN3 ELISA Kit (Human) (OKEH04449)  Polyclonal Antibody (Human), APC)
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human), APC  Polyclonal Antibody (Human), Biotinylated)
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human), Biotinylated  Polyclonal Antibody (Human), Cy3)
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human), Cy3  Polyclonal Antibody (Human), FITC)
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human), FITC  Polyclonal Antibody (Human), HRP)
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human), HRP  Polyclonal Antibody (Human), PE)
Actinin Alpha 3 (ACTN3) Polyclonal Antibody (Human), PE  Protein)
Human Actinin Alpha 3 (ACTN3) Protein  ELISA Kit)
Actinin Alpha 3 (ACTN3) ELISA Kit  CLIA Kit)
Actinin Alpha 3 (ACTN3) CLIA Kit