MB21D2 antibody (AbBy Fluor® 350)

Catalog No. ABIN1404933

Product Details anti-MB21D2 Antibody (AbBy Fluor® 350)

Target: MB21D2 (Mab-21 Domain Containing 2 (MB21D2))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MB21D2 antibody is conjugated to AbBy Fluor® 350

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf59/MB21D2

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 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 MB21D2

Target: MB21D2 (Mab-21 Domain Containing 2 (MB21D2))

Alternative Name: C3orf59 (MB21D2 Products)

Synonyms: C3orf59 antibody, 1600021P15Rik antibody, A430031N04 antibody, C87006 antibody, Mab-21 domain containing 2 antibody, chromosome 3 open reading frame 59 antibody, MB21D2 antibody, c3orf59 antibody, Mb21d2 antibody

Background:

Synonyms: Protein MB21D2, Mab-21 domain-containing protein 2, M21D2_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 C3orf59 gene product has been provisionally designated C3orf59 pending further characterization.