Anti-human alpha

Species Reactivity : Human (Homo sapiens)
UniProt : O43707
Abbreviation : ACTN4
Alternative Names : ACTININ-4; DKFZp686K23158; FSGS; FSGS1; actinin alpha4 isoform
Application : ELISA
Range : 0.78-50 ng/mL
Sensitivity : 0.32 ng/mL
Intra-AssayCV : ?5.2%
Inter-AssayCV : ?9.1%
Recovery : 1.01
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate ACTN4 in samples. An antibody specific for ACTN4 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyACTN4 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for ACTN4 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of ACTN4 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with m µLtiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. Alpha-actinin-4 is a nonmuscle, alpha actinin isoform which is concentrated in the cytoplasm, and tho µght to be involved in metastatic processes. Mutations in this gene have been associated with focal and segmental glomer µLosclerosis.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : Q08043
Abbreviation : ACTN3
Alternative Names : MGC117002; MGC117005;
Application : ELISA
Range : 1.56-100 ng/mL
Sensitivity : 0.62 ng/mL
Intra-AssayCV : ?4.3%
Inter-AssayCV : ?8.3%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate ACTN3 in samples. An antibody specific for ACTN3 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyACTN3 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for ACTN3 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of ACTN3 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Actinin, alpha 3, also known as ACTN3, is a protein which in humans is encoded by the ACTN3 gene.Alpha-actinin is an actin-binding protein with m µLtiple roles in different cell types. This gene expression is limited to skeletal muscle. It is localized to the Z-disc and analogous dense bodies, where it helps to anchor the myofibrillar actin filaments. Skeletal muscle is composed of long cylindrical cells called muscle fibers. There are two types of muscle fibers, slow twitch or muscle contraction (type I) and fast twitch (type II). Slow twitch fibers are more efficient in using oxygen to generate energy whilst fast twitch fibers are less efficient. However, fast twitch fibers fire more rapidly and generate more force.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P12814
Abbreviation : ACTN1
Alternative Names : FLJ40884; FLJ54432; F-actin cross-linking protein|actinin 1 smooth muscle|alpha-actinin 1
Application : ELISA
Range : 0.156-10 ng/mL
Sensitivity : 0.039 ng/mL
Intra-AssayCV : ?5.2%
Inter-AssayCV : ?9.8%
Recovery : 1
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate ACTN1 in samples. An antibody specific for ACTN1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyACTN1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for ACTN1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of ACTN1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with m µLtiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. Alpha-actinin-1 is a nonmuscle, cytoskeletal, alpha actinin isoform and maps to the same site as the structurally similar erythroid beta spectrin gene.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : N/A
Abbreviation : A-Actin
Alternative Names : N/A
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.2%
Inter-AssayCV : ?7.8%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate A-Actin in samples. An antibody specific for A-Actin has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyA-Actin present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for A-Actin is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of A-Actin bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Actin, alpha cardiac muscle 1 is a protein encoded by the ACTC1 gene.Actins are highly conserved proteins that are involved in various types of cell motility. Polymerization of glob µLar actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to four others.The protein encoded by this gene belongs to the actin family which is composed of three main groups of actin isoforms, alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. Defects in this gene have been associated with idiopathic dilated cardiomyopathy (IDC) and familial hypertrophic cardiomyopathy (FHC).
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P18825
Abbreviation : ADRA2C
Alternative Names : ADRA2L2; ADRA2RL2; ADRARL2; ALPHA2CAR; alpha-2C-adrenergic receptor|alpha2-AR-C4
Application : ELISA
Range : 0.625-40 ng/mL
Sensitivity : 0.237 ng/mL
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?8.9%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate ADRA2C in samples. An antibody specific for ADRA2C has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyADRA2C present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for ADRA2C is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of ADRA2C bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Alpha-2-adrenergic receptors include 3 highly homologous subtypes : alpha2A, alpha2B, and alpha2C. These receptors have a critical role in reg µLating neurotransmitter release from sympathetic nerves and from adrenergic neurons in the central nervous system. Studies in mouse revealed that both the alpha2A and alpha2C subtypes were required for normal presynaptic control of transmitter release from sympathetic nerves in the heart and from central noradrenergic neurons; the alpha2A subtype inhibited transmitter release at high stim µLation frequencies, whereas the alpha2C subtype mod µLated neurotransmission at lower levels of nerve activity.ADRa2C encodes the alpha2C subtype, which contains no introns in either its coding or untranslated sequences.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Cell Biology
Uniprot ID : A8K2U0
Species : Human
Former Code :
Alias : CPAMD9, DKFZp686C1729, DKFZp686D2011 DKFZp686G1812, DKFZp686L1821 DKFZp686O1010, FLJ16045, FLJ25179, FLJ39129, FLJ41597, FLJ41598, FLJ41607, C3 and PZP-like, alpha-2-macroglob µLin domain containin
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates
Detect Range : 9.38 ng/ml-600 ng/ml
Sensitivity : 2.34 ng/ml.
Antigen Name : alpha-2-macroglob µLin-like 1
Abbreviation : A2ML1
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 7-14 working days

Species Reactivity : Human (Homo sapiens)
UniProt : A8K2U0
Abbreviation : A2ML1
Alternative Names : CPAMD9; DKFZp686C1729; DKFZp686D2011; DKFZp686G1812; DKFZp686L1821; DKFZp686O1010; FLJ16045; FLJ25179; FLJ39129; FLJ41597; FLJ41598; FLJ41607; C3 and PZP-like; alpha-2-macroglob µLin domain containin
Application : ELISA
Range : 0.78-50 ng/mL
Sensitivity : 0.34 ng/mL
Intra-AssayCV : ?4.8%
Inter-AssayCV : ?6.5%
Recovery : 0.96
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate A2ML1 in samples. An antibody specific for A2ML1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyA2ML1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for A2ML1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of A2ML1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The alpha-macroglob µLin (AM) superfamily of proteins contains both complement components and protease inhibitors, including A2M and A2ML1. AM proteins display a unique trap mechanism of inhibition, by which the AM inhibitor undergoes a major conformational change upon its cleavage by a protease, thus trapping the protease and blocking it from subsequent substrate binding. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molec µLar weight substrates. Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P01023
Abbreviation : A2M
Alternative Names : CPAMD5; DKFZp779B086; FWP007; S863-7;
Application : ELISA
Range : 0.78-50 ng/mL
Sensitivity : 0.35 ng/mL
Intra-AssayCV : ?4.9%
Inter-AssayCV : ?7.4%
Recovery : 0.88
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate A2M in samples. An antibody specific for A2M has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyA2M present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for A2M is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of A2M bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Alpha2-macroglob µLin is a major serum protein with diverse functions, including inhibition of protease activity and binding of growth factors, cytokines, and disease factors. It is also a panproteinase inhibitor that is found immunohistochemically in neuritic plaques. Alpha-2-macroglob µLin is able to inactivate an enormous variety of proteinases (including serine-, cysteine-, aspartic- and metalloproteinases). Alpha-2-macroglob µLin has in its structure a 35 aminoacid "bait" region. Proteinases binding and cleaving the bait region become bound to alpha2M. The proteinase-?2M complex is recognised by macrophage receptors and cleared from the system
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : N/A
Abbreviation : SERPINF2
Alternative Names : A2AP; AAP; ALPHA-2-PI; API; PLI; OTTHUMP00000115656|alpha-2-antiplasmin|alpha-2-plasmin inhibitor|serine (or cysteine) proteinase inhibitor; clade F (alpha-2 antiplasmin; pigment epithelium derived
Application : ELISA
Range : 1.56-100 ng/mL
Sensitivity : 0.69 ng/mL
Intra-AssayCV : ?6.3%
Inter-AssayCV : ?8.5%
Recovery : 0.97
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate SERPINF2 in samples. An antibody specific for SERPINF2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySERPINF2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for SERPINF2 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of SERPINF2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : An inherited hemorrhagic diathesis due to plasmin inhibitor deficiency was described by Koie et al. (1978) in a 25-year-old Okinawa man. He had suffered prolonged bleeding and ecchymoses after minor trauma, spontaneous joint hemorrhage, and one episode of hemothorax. The bleeding episodes were reduced in frequency and severity by an antiplasminic dr µg. Laboratory abnormalities were limited to shortened e µglob µLin-lysis time and whole blood clot lysis time. No circ µLating alpha-2-plasmin inhibitor was found in the plasma. Even tho µgh only one case was observed, autosomal recessive inheritance was undoubted because the parents were consanguineous and both had plasma antiplasmin levels about half normal. The authors called the condition Miyasato disease after the proband's surname.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Cell Biology
Uniprot ID : Q2KJF1
Species : Human
Former Code : CSB-E11730h
Alias : A1B, ABG, DKFZp686F0970, GAB, HYST2477, alpha 1B-glycoprotein
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates
Detect Range : 62.5 ng/ml-4000 ng/ml
Sensitivity : 15.6 ng/ml
Antigen Name : alpha-1-B glycoprotein
Abbreviation : A1BG
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 7-14 working days

Species Reactivity : Human (Homo sapiens)
UniProt : Q2KJF1
Abbreviation : A1BG
Alternative Names : A1B; ABG; DKFZp686F0970; GAB; HYST2477; alpha 1B-glycoprotein
Application : ELISA
Range : 0.312-20 ng/mL
Sensitivity : 0.147 ng/mL
Intra-AssayCV : ?5.7%
Inter-AssayCV : ?7.9%
Recovery : 0.88
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate A1BG in samples. An antibody specific for A1BG has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyA1BG present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for A1BG is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of A1BG bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Alpha-1B-glycoprotein is present in normal ad µLt plasma at an average concentration of 22 mg/dl. Gahne et al. (1987) observed genetic polymorphism of A1B using one-dimensional horizontal polyacrylamide gel electrophoresis followed by Western blotting with specific antiserum. Three different phenotypes, designated 1-1 1-2, and 2-2, were observed. Family data supported the hypothesis that the three phenotypes are determined by 2 codominant alleles at an autosomal locus. In pigs the homologous locus is linked to malignant hyperthermia. Several other linkages in pigs and in horses s µggest that human chromosomes 19, 6, and 1 are 'candidate chromosomes' for bearing the human A1B.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).