CCDC37 antibody (AA 201-300) (HRP)

Catalog No. ABIN887657

The Rabbit Polyclonal anti-CCDC37 antibody has been validated for WB, ELISA, IHC (p) and IHC (fro). It is suitable to detect CCDC37 in samples from Human.

Quick Overview for CCDC37 antibody (AA 201-300) (HRP) (ABIN887657)

Target: CCDC37 (Coiled-Coil Domain Containing 37 (CCDC37))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC37 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-CCDC37 Antibody (HRP)

Binding Specificity: AA 201-300

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC37

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 CCDC37

Target: CCDC37 (Coiled-Coil Domain Containing 37 (CCDC37))

Alternative Name: CCDC37

Background:

Synonyms: CCD37_HUMAN, CCDC37, Coiled-coil domain containing 37, Coiled-coil domain-containing protein 37.

Background: CCDC37 is a 611 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding CCDC37 maps to human chromosome 3, which 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.

Gene ID: 348807