NCKAP1L anticorps (AA 1-100) (Alexa Fluor 488)

N° du produit ABIN1695906

Détail du produit anti-NCKAP1L anticorps (Alexa Fluor 488)

Antigène: NCKAP1L (NCK-Associated Protein 1-Like (NCKAP1L))

Épitope: AA 1-100

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NCKAP1L est conjugé à/à la Alexa Fluor 488

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human NCKAP1L/HEM1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur NCKAP1L

Antigène: NCKAP1L (NCK-Associated Protein 1-Like (NCKAP1L))

Autre désignation: NCKAP1L/HEM1 (NCKAP1L Produits)

Sujet:

Synonyms: 4930568P13Rik, AI463083, HEM1, Hematopoietic protein 1, HEMATOPOIETIC PROTEIN HEM-1, Hemp1, Membrane associated protein hem1, Membrane-associated protein HEM-1, NCK associated protein 1 like, Nck-associated protein 1-like, NCKAP1L, NCKPL_HUMAN.

Background: HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.

ID gène: 3071

Pathways: Regulation of Actin Filament Polymerization