SSUH2 antibody (AA 51-150) (AbBy Fluor® 350)

Catalog No. ABIN1693655

The Rabbit Polyclonal anti-SSUH2 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect SSUH2 in samples from Mouse and Rat.

Quick Overview for SSUH2 antibody (AA 51-150) (AbBy Fluor® 350) (ABIN1693655)

Target: SSUH2 (Ssu-2 Homolog (C. Elegans) (SSUH2))

Reactivity: Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SSUH2 antibody is conjugated to AbBy Fluor® 350

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

Product Details anti-SSUH2 Antibody (AbBy Fluor® 350)

Binding Specificity: AA 51-150

Cross-Reactivity: Mouse, Rat

Predicted Reactivity: Human,Dog,Sheep

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf32

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for SSUH2

Target: SSUH2 (Ssu-2 Homolog (C. Elegans) (SSUH2))

Alternative Name: C3orf32

Background:

Synonyms: chromosome 3 open reading frame 32, fls485, SSU-2, SSUH2, SSUH2 ssu-2 homolog C. elegans, uncharacterized protein C3orf32 homolog, SSUH2_HUMAN.

Background: C3orf32 (chromosome 3 open reading frame 32), also known as fls485, is a 353 amino acid protein encoded by a gene that maps to human chromosome 3p26.1. Chromosome 3 is made up of approximately 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.

Gene ID: 51066