CCDC93 antibody (AA 531-631) (Cy5)

Catalog No. ABIN888340

Product Details anti-CCDC93 Antibody (Cy5)

Target: CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))

Binding Specificity: AA 531-631

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC93 antibody is conjugated to Cy5

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

Cross-Reactivity: Rat

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC93

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 CCDC93

Target: CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))

Alternative Name: CCDC93 (CCDC93 Products)

Synonyms: 4633402D15Rik antibody, 9230102M16Rik antibody, coiled-coil domain containing 93 antibody, coiled-coil domain containing 93 L homeolog antibody, CCDC93 antibody, Ccdc93 antibody, ccdc93.L antibody

Background:

Synonyms: CCDC 93, Coiled-coil domain containing 93, FLJ10996, FLJ25197, MGC13033, CCD93_HUMAN.

Background: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC93 (coiled-coil domain containing 93) is a 631 amino acid protein that belongs to the CCDC93 family. CCDC93 is encoded by a gene located on human chromosome 2, which makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene.

Gene ID: 54520