C15orf40 antibody

Catalog No. ABIN7246064

Product Details anti-C15orf40 Antibody

Target: C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C15orf40 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Fusion protein of human C15orf40

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for C15orf40

Target: C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Alternative Name: C15orf40 (C15orf40 Products)

Synonyms: MGC89060 antibody, AI851475 antibody, C15orf40 antibody, c15orf40 antibody, chromosome 15 open reading frame 40 antibody, RIKEN cDNA 3110040N11 gene antibody, similar to RIKEN cDNA 3110040N11 antibody, chromosome 21 open reading frame, human C15orf40 antibody, chromosome 15 open reading frame 40 L homeolog antibody, C15orf40 antibody, c15orf40 antibody, 3110040N11Rik antibody, RGD1305713 antibody, C21H15orf40 antibody, c15orf40.L antibody

Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.

Molecular Weight:

Observed_MW: Refer to figures

Calculated_MW: 16 kDa

UniProt: Q8WUR7