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Chorionic Somatomammotropin Hormone 1 (Placental Lactogen) (CSH1) Peptide

CSH1 Reactivité: Humain Hôte: Synthetic BP, WB, IHC
N° du produit ABIN975362

Aperçu rapide pour Chorionic Somatomammotropin Hormone 1 (Placental Lactogen) (CSH1) Peptide (ABIN975362)

Antigène

CSH1 (Chorionic Somatomammotropin Hormone 1 (Placental Lactogen) (CSH1))

Origine

Humain

Source

  • 4
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-CSH1 antibody (Catalog #: ARP40350_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Indications d'application

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

    CSH1 (Chorionic Somatomammotropin Hormone 1 (Placental Lactogen) (CSH1))

    Sujet

    CSH1 is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, although the ratio of 1 to 2 increases by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome.The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation, an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, although the ratio of 1 to 2 increases by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome.

    Alias Symbols: PL, CSA, CS-1, CSMT, hCS-A

    Protein Interaction Partner: PRLR,PTPN12,SMAD2,SMAD4,SMAD9,POLR2A,SMAD3

    Protein Size: 217

    Poids moléculaire

    24 kDa

    ID gène

    1442

    NCBI Accession

    NM_001317, NP_001308

    UniProt

    P01243
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