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SHPK anticorps

Cet anticorps anti-SHPK est un anticorps Souris Monoclonal détectant SHPK dans WB, IF et FACS. Adapté pour Humain.
N° du produit ABIN2731603

Aperçu rapide pour SHPK anticorps (ABIN2731603)

Antigène

Voir toutes SHPK Anticorps
SHPK (Sedoheptulokinase (SHPK))

Reactivité

  • 24
  • 15
  • 14
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
Humain

Hôte

  • 19
  • 5
Souris

Clonalité

  • 20
  • 4
Monoclonal

Conjugué

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SHPK est non-conjugé

Application

  • 16
  • 6
  • 5
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

4E9
  • Attributs du produit

    Homo sapiens sedoheptulokinase (SHPK)

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogène

    Full length human recombinant protein of human SHPK(NP_037408) produced in HEK293 cell.

    Isotype

    IgG2a
  • Indications d'application

    WB 1:2000, IF 1:100, FLOW 1:100,

    Commentaires

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • Antigène

    SHPK (Sedoheptulokinase (SHPK))

    Autre désignation

    SHPK

    Sujet

    The protein encoded by this gene has weak homology to several carbohydrate kinases, a class of proteins involved in the phosphorylation of sugars as they enter a cell, inhibiting return across the cell membrane. Sequence variation between this novel gene and known carbohydrate kinases suggests the possibility of a different substrate, cofactor or changes in kinetic properties distinguishing it from other carbohydrate kinases. The gene resides in a region commonly deleted in cystinosis patients, suggesting a role as a modifier for the cystinosis phenotype. The genomic region is also rich in Alu repetitive sequences, frequently involved in chromosomal rearrangements. COMPLETENESS: complete on the 3' end.

    Poids moléculaire

    51.3 kDa

    ID gène

    23729

    NCBI Accession

    NM_013276

    HGNC

    23729

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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