C22orf13 antibody (AA 51-150) (Alexa Fluor 350)

Catalog No. ABIN1693654

Product Details anti-C22orf13 Antibody (Alexa Fluor 350)

Target: C22orf13 (GUCD1) (Guanylyl Cyclase Domain Containing 1 (GUCD1))

Binding Specificity: AA 51-150

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C22orf13 antibody is conjugated to Alexa Fluor 350

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

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C22orf13

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 C22orf13

Target: C22orf13 (GUCD1) (Guanylyl Cyclase Domain Containing 1 (GUCD1))

Alternative Name: C22orf13 (GUCD1 Products)

Synonyms: C22orf13 antibody, LLN4 antibody, 1110038D17Rik antibody, C17H22orf13 antibody, wu:fi27d12 antibody, zgc:152874 antibody, guanylyl cyclase domain containing 1 antibody, GUCD1 antibody, Gucd1 antibody, gucd1 antibody

Background:

Synonyms: C22orf13, CG13760 gene product [Drosophila melanogaster] homolog, Chromosome 22 open reading frame 13, CV013_HUMAN, LLN4, MGC1842, OTTHUMP00000198388, Protein LLN4, Uncharacterized protein C22orf13.

Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.

Gene ID: 83606