Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1980-1984  (2)
  • 1970-1974  (4)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 11 (1972), S. 2644-2653 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of immunogenetics 1 (1974), S. 0 
    ISSN: 1744-313X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: The genetic control of the antibody response to poly(Glu52Lys33Tyr15) was studied in twenty-five strains of inbred rats representing a wide variety of major histocompatibility groups. Direct linkage studies, and three subsidiary lines of evidence, demonstrated that the control was linked to the major histocompatibility locus. All of the low responders (Ag-B1, 3 and 6) made less than 65 μg of antibody/ml. In contrast, there were quantitatively significant differences among responders: the Ag-B2 group was a moderate responder (200–500 μg antibody/ml) and the Ag-B4 and Ag-B5 groups were high responders (700–1400 μg/ml). The ability to form antibody segregated with the major histocompatibility allele in the F2 and back-cross generations. Genetic factors other than those controlling the ability to respond influence the quantity of antibody formed: animals of the same genotype can make significantly different amounts of antibody, depending upon the crosses by which they acquire the major histocompatibility alleles.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of immunogenetics 1 (1974), S. 0 
    ISSN: 1744-313X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: Two genetically inbred strains of rats with new histocompatibility alleles—the KGH and WKA strains—were characterized. Neither the KGH nor WKA strain cells reacted with known Ag-B * specific antisera; specific antisera against these strains did not react with cells from any known Ag-B group; and there was no cross-reactivity between the histocompatibility antigens of the two strains. On the basis of these data, the KGH strain was assigned the Ag-B7 allele and the WKA strain, the Ag-B8 allele. Both strains were low responders to the test antigen poly(Glu52Lys33Tyr15). In various crosses, the antibody response segregated as expected, i.e. low response was associated with the Ag-B7 or Ag-B8 alleles in the F2 and backcross generations.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of immunogenetics 1 (1974), S. 0 
    ISSN: 1744-313X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: There is no evidence for genetic control of the antibody response to the d-amino acid polypeptide poly(dGlu52dLys33dTyr15) in contrast to the case of the l-isomer in which the antibody response is genetically controlled and linked to the major histocompatibility locus. There is also no crossreactivity between the l- and d-isomers of the polypeptide in the induction of the immune response. Aggregation of the l-isomer with methylated bovine serum albumin (MeBSA) abolished the pattern of genetic control by increasing antibody formation in the low responders and by decreasing it in the high responders. Aggregation of the d-isomer increased rather uniformly the antibody responses of all strains, except the moderately responding WF strain. The antibody response to the MeBSA in the aggregates was uniformly low, although there was a strain dependent variation in the antibody response to MeBSA alone.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In the rat, genes that control the expression of target antigens detected by cell-mediated lympholysis (CML) are present in the major histocompatibility complex (MHC). The relationship of these loci, CT and Ag-L, to each other and to other loci within the MHC is unknown. In this report, we demonstrate the existence of a CML target antigen in the (DA × BN)F1 anti-DA.11(BI) strain combination. The gene coding for this antigen is linked to the RT1 complex as indicated by the CML reactivity of targets from backcross and congenic animals. Inhibition studies demonstrated that this antigen has the widespread tissue distribution characteristic of class I antigens, and the gene coding for this CML antigen maps coincident with the RT1.E class I locus as indicated by the lysis of targets from the recombinant strains r10 and r11. The CML can be blocked by antisera directed against a product of the RT1.E locus. The locus controlling this CML reactivity, like CT and Ag-L, has been separated from RT1.A by recombination; unlike CT and Ag-L, the product of this CML locus appears to be identical with an RT1.E allelic product that has been serologically identified and biochemically characterized.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 13 (1981), S. 371-379 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The loci in the major histocompatibility complex (MHC) of the rat which code for class I and class II antigens—RT1.A and RT1.B, respectively — have previously been separated by laboratory-derived recombinants and by observations in inbred and wild rats. Closely linked to the MHC is the growth and reproduction complex (Grc) which contains genes influencing body size (dw-3) and fertility (ft). These phenotypic markers were used in this study to orient the A and B loci of the MHC. Two recombinants were used for mapping. The BIL(R1) animal is a recombinant between the MHC and Grc, and it carries the haplotype RT1.A lBlGrc+. The r10 animal is an intra-MHC recombinant, and it has the haplotype RT1.A nB1 Grc. These recombinants were characterized serologically, by mixed lymphocyte reactivity, by immune responsiveness to poly (Glu52Lys33Tyr15) and by the presence of the dw-3 gene. The data demonstrate that the gene order of the loci is: dw-3-RT1.B-RT1.A.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...