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 Update : 25-09-2008
 

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All hemoglobin Controls

ACS

ACS, Inc. is a small, closely held corporation dedicated solely to inventing and manufacturing diagnostic controls, reagents and tests. Since its founding in 1978, ACS has earned an excellent reputation as an OEM manufacturer. Our in-depth knowledge of manufacturing extremely stable protein & enzyme products either in lyophilized or liquid format has allowed us to move into a retail market and compete successfully with giants in the field.

Hemoglobin Assays and Controls
Glycohemoglobin Controls, Normal & Elevated The normal level glycohemoglobin product is a stabilized oxy hemoglobin control with values between 6.0% and 8.0%. The elevated control has a glycohemoglobin level between 11% and 15%. The values are assigned by electrophoresis and affinity chromatography methods. These product perform very well in weak cation exchange HPLC. Stability is excellent, at least 10 days after reconstitution, 21 days frozen after reconstitution and for two years as a lyophilized powder.

 

  • HC-101 6 X 0.5 ml normal controls
  • HC-101EL 6 X 0.5 ml elevated controls

     

    Variant Hemoglobin Control, AFSC & NAFSC
    ACS’s Variant Hemoglobin Control, AFSC and NAFSC are useful controls for any electrophoresis screening procedure where variant hemoglobins are expected. The stabilized oxyhemoglobin based AFSC control has values for A, F, S, and C of approximately 40%, 25%, 20% and 15% respectively and the stabilized, oxyhemoglobin based NAFSC control has values for N-Baltimore, A, F,S, and C of approximately 34%, 44%, 6%, 6% and 9% respectively. The products are stable for 10 days after reconstitution, for 21 days frozen after reconstitution and for two years unreconstituted and refrigerated.

     

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  • HC-102 6 X 0.5 ml AFSC Control
  • HC-102N 6 X 0.5 ml NAFSC Control

     

    Variant Hemoglobin Control, HAFS
    The blocks and empty spaces represent the genes for alpha-globin synthesis. Hemoglobin H represents an excess beta chain production and is a hemoglobin tetramer of beta chains. This is caused by a decreased production of alpha-globin chains causing a production mismatch. Because the amount of Hemoglobin H is rather low in heterozygous patients, ACS’s control is formulated with A, F, S and C and is rather out of balance with low (but detectable) H, markedly high A, and lower F, S and C values. This control allows the laboratory to test their procedures to determine if they can detect Hemoglobin H thereby helping in the detection of alpha thalassemia. The product is stable for 10 days after reconstitution, for 21 days frozen after reconstitution and for two years unreconstituted and refrigerated.

     

  • HC-102H 6 X 0.5 ml HAFSC Control

     

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    Variant Hemoglobin Control, AF
    ACS’s Variant Hemoglobin Control, AF is useful in laboratories doing hemoglobin electrophoresis screening of newborns. The control performs on both alkaline electrophoresis and acid citrate agar media. The stabilized, oxyhemoglobin based Variant Hemoglobin Control, AF has values for A and F of about 60% and 40%, respectively. The stability is assured for at least 10 days reconstituted, 21 days frozen after reconstitution and the control has a two year refrigerated shelf life when unreconstituted.

     

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    Variant Hemoglobin Control, AS
    ACS’s Variant Hemoglobin Control, AS is useful in laboratory screenings for sickle cell trait and disease. The control performs on both alkaline electrophoresis and acid citrate agar media. The stabilized, oxyhemoglobin based Variant Hemoglobin Control, AS has values for A and S of about 60% and 40% respectively. Stability is assured for at least 10 days reconstituted, 21 days frozen after reconstitution and the control has a two year refrigerated shelf life when unreconstituted.

     

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    Variant Hemoglobin Control, AC
    ACS’s Variant Hemoglobin Control, AC is useful in confirming the presence of variant hemoglobin C in populations where C and E occur and in the presence of other hemoglobins such as elevated hemoglobin A2. The control performs on both alkaline electrophoresis and acid citrate agar media. The stabilized, oxyhemoglobin based Variant Hemoglobin Control, AC has values for A and C of about 60% and 40% respectively. Stability is assured for at least 10 days reconstituted, 21 days frozen after reconstitution and the control has a two year refrigerated shelf life when unreconstituted.

     

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    Hemoglobin A2 Control, Normal & Elevated
    The measurement of hemoglobin A2 is important in the diagnosis of thalessemia. The most commonly used diagnostic procedures are alkaline cellulose electrophoresis and column chromatography. ACS’s normal and elevated A2 controls are specifically prepared to be useful in both procedures. The total hemoglobin is adjusted to about 4.0 gm/dl and the normal control contains from 1.5%-2.5% A2, while the elevated contains 3.5% to 5.0%. The reconstituted controls can be applied directly in either procedure without further dilution. For procedures which measure A2 in the presence of hemoglobin S, please inquire. The bulk product may also be order OEM to dispense and lyophilized on location (minimum 1 liter).

    • HC-111 6X0.5 ml normal
    • HC-112 6X0.5 ml elevated

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    Variant Hemoglobin Control, AE
    Hemoglobin E is a fairly rare hemoglobinopathy in the United States. However, it occurs in the 30– 50 million person range in Asia, mainly among southeast Asian peoples. Therefore, a high incidence of hemoglobin E is to be expected among such populations both in America and in Europe. Because of the overlap between hemoglobin E and beta thalassemia, there may be severe clinical symptoms amongst heterozygous E patients due to the combined hemoglobinopathies (E & beta thalassemia). Due to the electrophoresis mobility properties, structural stability and other physical characteristics of these hemoglobins, good technique and appropriate controls are essential in the correct identification of these hemoglobinopathies. Care also should be taken to properly identify and quantitate hemoglobin A2 when thalassemia is suspected. ACS makes a heterozygous quality control sample. The donor AE has been carefully tested and properly identified to assure analysts that a proper E hemoglobin in present.

    • HC-117 6X0.5 ml

     

    Variant Hemoglobin Controls, AFC & AFS
    ACS’s Variant Hemoglobin Control, AFC is useful in confirming the presence of variant hemoglobin C in populations where C and E occur and in the presence of other hemoglobins such as elevated hemoglobin A2. ACS’s Variant Hemoglobin Control, AFS is useful in laboratories screening for sickle cell trait and disease. The controls perform on both alkaline electrophoresis and acid citrate agar mediums. AFC and AFS are stabilized, oxyhemoglobin based Variant Hemoglobin Controls. Stability is assured for at least 10 days reconstituted, 21 days frozen after reconstitution and the control has a two year refrigerated shelf life when unreconstituted.

    • HC-118 AFS 6 X 0.5 ml
    • HC-119 AFC 6 X 0.5 ml
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    Variant Hemoglobin Control, AD
    Although both hemoglobin D disease and trait hemoglobin AD are extremely rare, the importance of using controls is highlighted by the fact that hemoglobin S and hemoglobin D migrate similarly upon alkaline (pH 8.6) electrophoresis. This is so because both hemoglobin S and D arise from single, similarly charged amino acid substitutions on the beta-globin chain. The substitution is at position six in hemoglobin S and 121 for hemoglobin D. Hemoglobin D doesn’t sickle using the standard laboratory techniques but does have a higher than normal oxygen affinity. Using selective laboratory techniques and controls allows the correct diagnosis of hemoglobin D trait or disease.

    • HC-120 6 X 0.5 ml

     

    Variant Hemoglobin Controls, Fractions
    ACS’s Variant Hemoglobin Control, Fractions contains one vial each of AS, AC, AF and A2 stabilized, oxyhemoglobin based Variant Hemoglobin Controls. AC helps to confirm the presence of variant hemoglobin C in populations where C and E occur. The measurement of A2 is important in the diagnosis of thalessemia. AS is useful in laboratories screening for sickle cell trait and disease. AF aids laboratories involved in the screening of newborns. The controls perform on both alkaline electrophoresis and acid citrate agar media. Stability is assured for at least 10 days reconstituted, 21 days frozen after reconstitution and the control has a two year refrigerated shelf life when unreconstituted.

     

    • HC-121 AS 1 X 0.5 ml,
    • HC-121 AF 1 X 0.5 ml,
    • HC-121 AC 1 X 0.5 ml, 
    • HC-121 A2 1 X 0.5 ml
     

    Quik-Sep® Hemoglobin F Assay Alkali Denaturation
    ACS Quik-Sep® Hemoglobin F Assay is designed for accurate quantitation of adult hemoglobin F in ranges from 2% to 40% by alkali denaturation. The ACS Hemoglobin Assay is based on the ability of hemoglobin F to resist denaturation under alkaline conditions. Most hemoglobins can be denatured at a base pH and then precipitated with ammonium sulfate. Fetal hemoglobin remains soluble and can be readily quantified using a standard laboratory spectrophotometer. Accurate measurement can be useful in helping the physician diagnose certain hemoglobinopathies and thalassemias. The Quik-Sep® Kit contains potassium cyanide, cyanmethemoglobin (Drabkin’s reagent), sodium hydroxide, ammonium sulfate and 50 filter columns.  


       
    • HK-1050, 50 tests Contains: Potassium Cyanide (2%), Cyanmethemoglobin (Drabkin’s) Reagent, Sodium Hydroxide, Ammonium Sulfate, Filter Columns

     

    Variant Hemoglobin Control, F Normal & Elevated
    ACS’s Variant Hemoglobin Control, F is an useful control for alkali denaturation hemoglobin screening. The normal control has an F hemoglobin approximately that of normal patients <2%, while the elevated control has an F hemoglobin level of approximately 8.5%. The control is designed for use on the ACS Quik-Sep® Hemoglobin Assay Kit (alkali denaturation) but performs on both alkaline electrophoresis and acid citrate agar mediums. Stability is assured for at least 10 days. Reconstituted, 21 days frozen after reconstitution and for two years as a lyophilized powder.

    Hemoglobin F Control

     

     

    • HC-106 6 x 0.5 ml
    • HC-106EL 6 X 0.5 ml  

     

     

      

    Hemoglobin, Galactose-1-Phosphate Uridyl Transferase Control, Normal & Depressed
    ACS’s Gal-1-PUT Control is hemoglobin based and useful in screening and quantitative assays used to aid the diagnosis of galactosssemia. The Gal-1-PUT Control contains Gal-1-PUT in a stabilized oxyhemoglobin base with either normal or depressed levels of enzyme in normal levels of hemoglobin. Stability is assured for at least 10 days when the control is reconstituted, 21 days frozen after reconstitution and for two years when refrigerated and unreconstituted. Approved OEM customers can order quantities (minimum of 1 liter ) to dispense and lyophilized at their own facilities.

     

    • HC-107 6 X 0.5 ml Normal Controls
    • HC-107DE 6 X 0.5 ml Depressed Controls
    • Both are available OEM as a bulk liquid

     

    Hemoglobin, Erythro-6-Dehydrogenase: Glucose-6-Phosphate Dehydrogenase Controls, Normal, Intermediate and Depressed
    ACS’s Hemoglobin based G-6-PDH Control is useful in tests designed to detect G-6-PDH deficiencies and in the management of drug sensitivities related to this deficiency. The controls, normal, intermediate and depressed, consist of stabilized oxyhemoglobin bases and adjusted levels of G-6-PDH. All three controls perform remarkably well in kinetic, visual or fluorescent procedures. Stability is at least 5 days reconstituted, 21 days frozen after reconstitution and two years as a lyophilized powder. The bulk product is available to OEM customers (minimum quantity: 1 liter) to be dispensed and lyophilized in house.

    • HC-108 6 X 0.5 ml Normal Controls
    • HC-108IN 6 X 0.5 ml Intermediate Controls
    • HC-108DE 6 X 0.5 ml Depressed Controls
    • All are available OEM as a bulk liquid

     

    Hemoglobin Control, Total
    ACS’s Total Hemoglobin Control is specifically designed to test the efficacy of hemoglobin tests such as cyanmethemoglobin. These reagents frequently loose their potency and yield inaccurate values as they age. Using a pre-prepared standard control assay will not detect this problem if the hemoglobin is in the measured chemical form before it is added to the reagent. ACS’s Total Hemoglobin Control fully checks assays reagents since it is composed of nearly all oxyhemoglobin. Values can be adjusted to range from very low to well above normal expected values. The higher concentration material can be used as a linearity verifier.

    • HC-110 6 X 3.0 Total Hemoglobin Controls Normal
    • HC-110LIN 6 X 3.0 Linearity Total Hemoglobin Controls
    • Total Hemoglobin is available as an OEM bulk liquid

     

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