CCDC22 antibody (AA 525-627) (Cy7)

Catalog No. ABIN887507

The Rabbit Polyclonal anti-CCDC22 antibody is suitable to detect CCDC22 in samples from Human. It has been validated for WB, IF (cc) and IF (p).

Quick Overview for CCDC22 antibody (AA 525-627) (Cy7) (ABIN887507)

Target: CCDC22 (Coiled-Coil Domain Containing 22 (CCDC22))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC22 antibody is conjugated to Cy7

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

Product Details anti-CCDC22 Antibody (Cy7)

Binding Specificity: AA 525-627

Purpose: CCDC22 Polyclonal Antibody, Cy7 Conjugated

Cross-Reactivity: Rat

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC22

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000), 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, 0.02 % 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 CCDC22

Target: CCDC22 (Coiled-Coil Domain Containing 22 (CCDC22))

Alternative Name: CCDC22

Background:

Synonyms: AI481216, CCD22_HUMAN, Ccdc22.

Background: This gene encodes a protein containing a coiled-coil domain. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. Localization of the orthologous rat protein suggests that it may play a role in neuronal injury response. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2011].

Gene ID: 28952