FAM62B anticorps (AA 801-921) (Alexa Fluor 488)

N° du produit ABIN1388704

Détail du produit anti-FAM62B anticorps (Alexa Fluor 488)

Antigène: FAM62B (ESYT2) (Extended Synaptotagmin 2 (ESYT2))

Épitope: AA 801-921

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM62B est conjugé à/à la Alexa Fluor 488

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

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ESYT2/FAM62B

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 FAM62B

Antigène: FAM62B (ESYT2) (Extended Synaptotagmin 2 (ESYT2))

Autre désignation: ESYT2/FAM62B (ESYT2 Produits)

Synonymes: anticorps CHR2SYT, anticorps E-Syt2, anticorps FAM62B, anticorps 2410017M09Rik, anticorps 4921504I16Rik, anticorps D12Ertd551e, anticorps Fam62b, anticorps extended synaptotagmin 2, anticorps extended synaptotagmin-like protein 2, anticorps ESYT2, anticorps Esyt2

Sujet:

Synonyms: Chr2 synaptotagmin, CHR2SYT, E Syt2, ESYT 2, ESYT2, Extended synaptotagmin 2, Extended synaptotagmin like protein 2, FAM 62B antibody Family with sequence similarity 62 C2 domain containing member B, Family with sequence similarity 62 member B, KIAA1228, Protein FAM62B, ESYT2_HUMAN.

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.