GLT8D2 anticorps (AA 85-180) (Cy5)

N° du produit ABIN1416174

Cet anticorps anti-GLT8D2 est un anticorps Lapin Polyclonal détectant GLT8D2 dans WB, IF (cc) et IF (p). Adapté pour Humain.

Aperçu rapide pour GLT8D2 anticorps (AA 85-180) (Cy5) (ABIN1416174)

Antigène: GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GLT8D2 est conjugé à/à la Cy5

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

Détail du produit anti-GLT8D2 anticorps (Cy5)

Épitope: AA 85-180

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Cow,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GLT8D2

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 GLT8D2

Antigène: GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))

Autre désignation: GLT8D2

Sujet:

Synonyms: GALA4A, GL8D2_HUMAN, GLT8D2, Glycosyltransferase 8 domain containing 2, Glycosyltransferase 8 domain-containing protein 2, Gycosyltransferase.

Background: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.

ID gène: 83468