ESYT3 antibody (AA 101-200) (Biotin)

Catalog No. ABIN1395535

This Rabbit Polyclonal antibody specifically detects ESYT3 in ELISA, IHC (fro) and IHC (p). It exhibits reactivity toward Rat.

Quick Overview for ESYT3 antibody (AA 101-200) (Biotin) (ABIN1395535)

Target: ESYT3 (Extended Synaptotagmin-Like Protein 3 (ESYT3))

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ESYT3 antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-ESYT3 Antibody (Biotin)

Binding Specificity: AA 101-200

Cross-Reactivity: Rat

Predicted Reactivity: Human,Mouse,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM62C

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for ESYT3

Target: ESYT3 (Extended Synaptotagmin-Like Protein 3 (ESYT3))

Alternative Name: FAM62C

Background:

Synonyms: CHR3SYT, E Syt3, ESYT3, Extended synaptotagmin 3, Extended synaptotagmin-like protein 3, ESYT3_HUMAN.

Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The FAM62C gene product has been provisionally designated FAM62C pending further characterization.