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ALDH1L1 anticorps (AA 282-424)

Cet anticorps anti-ALDH1L1 est un anticorps Lapin Polyclonal détectant ALDH1L1 dans WB, IHC, IF, ELISA, FACS et ICC. Adapté pour Humain, Souris, Rat et Singe.
N° du produit ABIN7601093

Aperçu rapide pour ALDH1L1 anticorps (AA 282-424) (ABIN7601093)

Antigène

Voir toutes ALDH1L1 Anticorps
ALDH1L1 (Aldehyde Dehydrogenase 1 Family, Member L1 (ALDH1L1))

Reactivité

  • 46
  • 31
  • 22
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
Humain, Souris, Rat, Singe

Hôte

  • 27
  • 27
  • 2
Lapin

Clonalité

  • 34
  • 23
Polyclonal

Conjugué

  • 36
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ALDH1L1 est non-conjugé

Application

  • 31
  • 24
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  • 9
  • 8
  • 5
  • 2
  • 1
  • 1
  • 1
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  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), ELISA, Flow Cytometry (FACS), Immunocytochemistry (ICC)
  • Épitope

    • 6
    • 5
    • 4
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    • 2
    • 1
    • 1
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    • 1
    • 1
    AA 282-424

    Fonction

    Anti-ALDH1L1 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-ALDH1L1 Antibody Picoband® (ABIN7601093). Tested in ELISA, Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human, Monkey, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human ALDH1L1 recombinant protein (Position: N282-L424).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.25 μg/mL, Human, Mouse, Rat, Monkey
    Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human, Mouse, Rat
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Champion, K. M., Cook, R. J., Tollaksen, S. L., Giometti, C. S. Identification of a heritable deficiency of the folate-dependent enzyme 10-formyltetrahydrofolate dehydrogenase in mice. Proc. Nat. Acad. Sci. 91: 11338-11342, 1994. 2. Gross, M. B. Personal Communication. Baltimore, Md. 11/2/2010. 3. Hong, M., Lee, Y., Kim, J. W., Lim, J. S., Chang, S. Y., Lee, K. S., Paik, S. G., Choe, I. S. Isolation and characterization of cDNA clone for human liver 10-formyltetrahydrofolate dehydrogenase. Biochem. Molec. Biol. Int. 47: 407-415, 1999.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.01 mg 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

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Antigène

    ALDH1L1 (Aldehyde Dehydrogenase 1 Family, Member L1 (ALDH1L1))

    Autre désignation

    ALDH1L1

    Sujet

    Synonyms: Type I iodothyronine deiodinase, 5DI, DIOI, Type 1 DI, Type-I 5'-deiodinase, DIO1, ITDI1, TXDI1

    Tissue Specificity: Widely expressed in adult (at protein level) and fetal tissues.

    Background: 10-formyltetrahydrofolate dehydrogenase is an enzyme that in humans is encoded by the ALDH1L1 gene. The protein encoded by this gene catalyzes the conversion of 10-formyltetrahydrofolate, NADP, and water to tetrahydrofolate, NADPH, and carbon dioxide. The encoded protein belongs to the aldehyde dehydrogenase family and is responsible for formate oxidation in vivo. Deficiencies in this gene can result in an accumulation of formate and subsequent methanol poisoning.

    Poids moléculaire

    97 kDa

    ID gène

    10840

    UniProt

    O75891
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