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TSPYL1 anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement TSPYL1 dans WB. Il présente une réactivité envers Humain et a été mentionné dans 5+ publications.
N° du produit ABIN1881952

Aperçu rapide pour TSPYL1 anticorps (C-Term) (ABIN1881952)

Antigène

Voir toutes TSPYL1 Anticorps
TSPYL1 (TSPY-Like 1 (TSPYL1))

Reactivité

  • 24
  • 8
Humain

Hôte

  • 21
  • 3
Lapin

Clonalité

  • 23
  • 1
Polyclonal

Conjugué

  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TSPYL1 est non-conjugé

Application

  • 17
  • 9
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB40829
  • Épitope

    • 8
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 343-372, C-Term

    Homologie

    M

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This TSPYL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 343-372 amino acids from the C-terminal region of human TSPYL1.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Date de péremption

    6 months
  • Vinci, Brauner, Tar, Rouba, Sheth, Sheth, Ravel, McElreavey, Bashamboo: "Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility." dans: Fertility and sterility, Vol. 92, Issue 4, pp. 1347-50, (2009) (PubMed).

    de Andrade, Peterson, Cunha, Moreira, Fattori, Saad, Costa: "Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster." dans: Blood cells, molecules & diseases, Vol. 37, Issue 2, pp. 82-90, (2006) (PubMed).

    Hering, Frade-Martinez, Bajanowski, Poets, Tschentscher, Riess: "Genetic investigation of the TSPYL1 gene in sudden infant death syndrome." dans: Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 8, Issue 1, pp. 55-8, (2006) (PubMed).

    Wang, Yoon, Oh, Jeon, Kim, Kim, Byun, Yang, Kim, Kim, Yeom, Yoo, Kim, Kim: "Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags." dans: Biochemical and biophysical research communications, Vol. 345, Issue 3, pp. 1022-32, (2006) (PubMed).

    Puffenberger, Hu-Lince, Parod, Craig, Dobrin, Conway, Donarum, Strauss, Dunckley, Cardenas, Melmed, Wright, Liang, Stafford, Flynn, Morton, Stephan: "Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 101, Issue 32, pp. 11689-94, (2004) (PubMed).

  • Antigène

    TSPYL1 (TSPY-Like 1 (TSPYL1))

    Autre désignation

    TSPYL1

    Sujet

    The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).

    Poids moléculaire

    49192

    NCBI Accession

    NP_003300

    UniProt

    Q9H0U9
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