C1QL2 antibody (FITC)

Catalog No. ABIN1404704

The Rabbit Polyclonal anti-C1QL2 antibody has been validated for WB and IF (p). It is suitable to detect C1QL2 in samples from Human, Mouse and Rat.

Quick Overview for C1QL2 antibody (FITC) (ABIN1404704)

Target: C1QL2 (Complement Component 1, Q Subcomponent-Like 2 (C1QL2))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C1QL2 antibody is conjugated to FITC

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

Product Details anti-C1QL2 Antibody (FITC)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1QL2/C1QTNF10

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 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 C1QL2

Target: C1QL2 (Complement Component 1, Q Subcomponent-Like 2 (C1QL2))

Alternative Name: C1QTNF10

Background:

Synonyms: C1q and tumor necrosis factor related protein 10, C1q domain containing protein, C1QL2, C1QL2_HUMAN, C1QTNF10, Complement C1q-like protein 2, Complement component 1, q subcomponent-like 2, CTRP10, gliacolin like.

Background: C1qL2, also known as CTRP10 or C1QTNF10, is a 287 amino acid secreted protein that contains one C1q domain and one collagen-like domain. C1qL2 belongs to a large family of multimeric proteins with a signature globular domain homologous to C1QA. These proteins also share structural homology with TNF family members. The gene that encodes C1qL2 consists of approximately 2,653 bases and maps to human chromosome 2q14.2. Consisting of 237 million bases, chromosome 2 encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid 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 due to mutations in the ALMS1 gene.

Gene ID: 165257