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polyclonal antibody against lif  (R&D Systems)


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    Structured Review

    R&D Systems polyclonal antibody against lif
    Polyclonal Antibody Against Lif, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 25 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/polyclonal antibody against lif/product/R&D Systems
    Average 94 stars, based on 25 article reviews
    polyclonal antibody against lif - by Bioz Stars, 2026-03
    94/100 stars

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    R&D Systems polyclonal antibody against human lif
    Detection of <t>LIF</t> transcripts in cultured human liver myofibroblasts. ( A ): Northern blot. Total RNA from cultured human liver myofibroblasts was hybridized with a cDNA probe to human LIF. A single 4.5 kb band was observed; ( B ) and ( C ): RT-PCR. Total RNA was subjected to reverse transcription then to PCR with the <t>hLIF-D3/hLIF-N4</t> ( B ) or with the hLIF-M3/hLIF-N4 primers ( C ).
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    Santa Cruz Biotechnology affinity purified polyclonal antibody raised against a peptide mapping at the amino terminus of human lif
    Detection of <t>LIF</t> transcripts in cultured human liver myofibroblasts. ( A ): Northern blot. Total RNA from cultured human liver myofibroblasts was hybridized with a cDNA probe to human LIF. A single 4.5 kb band was observed; ( B ) and ( C ): RT-PCR. Total RNA was subjected to reverse transcription then to PCR with the <t>hLIF-D3/hLIF-N4</t> ( B ) or with the hLIF-M3/hLIF-N4 primers ( C ).
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    Detection of LIF transcripts in cultured human liver myofibroblasts. ( A ): Northern blot. Total RNA from cultured human liver myofibroblasts was hybridized with a cDNA probe to human LIF. A single 4.5 kb band was observed; ( B ) and ( C ): RT-PCR. Total RNA was subjected to reverse transcription then to PCR with the hLIF-D3/hLIF-N4 ( B ) or with the hLIF-M3/hLIF-N4 primers ( C ).

    Journal: Comparative Hepatology

    Article Title: Expression of leukemia inhibitory factor (LIF) and its receptor gp190 in human liver and in cultured human liver myofibroblasts. Cloning of new isoforms of LIF mRNA

    doi: 10.1186/1476-5926-3-10

    Figure Lengend Snippet: Detection of LIF transcripts in cultured human liver myofibroblasts. ( A ): Northern blot. Total RNA from cultured human liver myofibroblasts was hybridized with a cDNA probe to human LIF. A single 4.5 kb band was observed; ( B ) and ( C ): RT-PCR. Total RNA was subjected to reverse transcription then to PCR with the hLIF-D3/hLIF-N4 ( B ) or with the hLIF-M3/hLIF-N4 primers ( C ).

    Article Snippet: A commercially available polyclonal antibody against human LIF (R&D Systems, Minneapolis, Minnesota, USA), and different monoclonal antibodies against gp190, previously described [ ], were used at concentrations optimised on control tissues.

    Techniques: Cell Culture, Northern Blot, Reverse Transcription Polymerase Chain Reaction, Reverse Transcription

    Sequence of LIF-D, M and T isoforms. Exons D, M and T are the 3 alternate first exons. Primers used for PCR are underlined. Primers hLIF-M2, M3 and M5 cover the same sequence but differ because of the presence or the absence of restriction sites.

    Journal: Comparative Hepatology

    Article Title: Expression of leukemia inhibitory factor (LIF) and its receptor gp190 in human liver and in cultured human liver myofibroblasts. Cloning of new isoforms of LIF mRNA

    doi: 10.1186/1476-5926-3-10

    Figure Lengend Snippet: Sequence of LIF-D, M and T isoforms. Exons D, M and T are the 3 alternate first exons. Primers used for PCR are underlined. Primers hLIF-M2, M3 and M5 cover the same sequence but differ because of the presence or the absence of restriction sites.

    Article Snippet: A commercially available polyclonal antibody against human LIF (R&D Systems, Minneapolis, Minnesota, USA), and different monoclonal antibodies against gp190, previously described [ ], were used at concentrations optimised on control tissues.

    Techniques: Sequencing

    RT-PCR analysis of LIF-M expression in various cell lines and in human liver. ( A ): LIF-M expression was analyzed with the hLIF-M2 and hLIF-3N primers: Line 1, human liver myofibroblasts; Line 2, HepG2; Line 3, Hep3B; Line 4, HuH7; Line 5, HEK293. Product sizes are shown in bp; ( B ): normal human liver samples. LIF-D expression was analyzed with the hLIF-D3 and hLIF-N4 primers in 4 different samples. The same samples also expressed LIF-M (not shown). Product sizes are shown in bp; ( C ): diseased human liver samples. In that case, LIF-M expression was analyzed with the hLIF-M3 and hLIF-4N primers in 4 cases of cirrhotic liver. The same samples also expressed LIF-D (not shown). Product sizes are shown in bp; ( D ): semi-quantitation of LIF-D and s-LIF-D expression in a human liver myofibroblasts sample. LIF-D expression was analyzed with the hLIF-D3 and hLIF-N4 primers. The left part shows the migration pattern of the PCR-amplified products with the number of cycles above and the size of the products indicated by arrows, in bp. The graph on the right shows the signal quantification. Similar results were obtained with LIF-M.

    Journal: Comparative Hepatology

    Article Title: Expression of leukemia inhibitory factor (LIF) and its receptor gp190 in human liver and in cultured human liver myofibroblasts. Cloning of new isoforms of LIF mRNA

    doi: 10.1186/1476-5926-3-10

    Figure Lengend Snippet: RT-PCR analysis of LIF-M expression in various cell lines and in human liver. ( A ): LIF-M expression was analyzed with the hLIF-M2 and hLIF-3N primers: Line 1, human liver myofibroblasts; Line 2, HepG2; Line 3, Hep3B; Line 4, HuH7; Line 5, HEK293. Product sizes are shown in bp; ( B ): normal human liver samples. LIF-D expression was analyzed with the hLIF-D3 and hLIF-N4 primers in 4 different samples. The same samples also expressed LIF-M (not shown). Product sizes are shown in bp; ( C ): diseased human liver samples. In that case, LIF-M expression was analyzed with the hLIF-M3 and hLIF-4N primers in 4 cases of cirrhotic liver. The same samples also expressed LIF-D (not shown). Product sizes are shown in bp; ( D ): semi-quantitation of LIF-D and s-LIF-D expression in a human liver myofibroblasts sample. LIF-D expression was analyzed with the hLIF-D3 and hLIF-N4 primers. The left part shows the migration pattern of the PCR-amplified products with the number of cycles above and the size of the products indicated by arrows, in bp. The graph on the right shows the signal quantification. Similar results were obtained with LIF-M.

    Article Snippet: A commercially available polyclonal antibody against human LIF (R&D Systems, Minneapolis, Minnesota, USA), and different monoclonal antibodies against gp190, previously described [ ], were used at concentrations optimised on control tissues.

    Techniques: Reverse Transcription Polymerase Chain Reaction, Expressing, Quantitation Assay, Migration, Amplification