ESYT1 anticorps (AA 651-750)

N° du produit ABIN1387363

Détail du produit anti-ESYT1 anticorps

Antigène: ESYT1 (Extended Synaptotagmin-Like Protein 1 (ESYT1))

Épitope: AA 651-750

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ESYT1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Réactivité croisée: Humain, Souris

Homologie: Rat,Dog,Cow,Pig,Horse,Rabbit,Monkey

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ESYT1/FAM62A

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur ESYT1

Antigène: ESYT1 (Extended Synaptotagmin-Like Protein 1 (ESYT1))

Autre désignation: ESYT1/FAM62A (ESYT1 Produits)

Synonymes: anticorps FAM62A, anticorps fam62a, anticorps si:ch211-239j9.4, anticorps DKFZp459I1628, anticorps MBC2, anticorps Fam62a, anticorps Mbc2, anticorps vp115, anticorps extended synaptotagmin 1, anticorps extended synaptotagmin-like protein 1b, anticorps extended synaptotagmin-like protein 1, anticorps ESYT1, anticorps esyt1b, anticorps Esyt1

Sujet:

Synonyms: Extended synaptotagmin 1, KIAA0747, E Syt1, E-Syt1, Esyt1, ESYT1_HUMAN, Extended synaptotagmin like protein 1, Extended synaptotagmin-1, Family with sequence similarity 62 C2 domain containing member A, Family with sequence similarity 62 member A, MBC2, Membrane bound C2 domain containing protein, Membrane-bound C2 domain-containing protein, Protein FAM62A.

Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.