C1QL2 anticorps (Biotin)

N° du produit ABIN1404703

Détail du produit anti-C1QL2 anticorps (Biotin)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C1QL2 est conjugé à/à la Biotin

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

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

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur C1QL2

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

Autre désignation: C1QTNF10 (C1QL2 Produits)

Synonymes: anticorps C1QTNF10, anticorps CTRP10, anticorps BC040774, anticorps complement C1q like 2, anticorps complement component 1, q subcomponent-like 2, anticorps C1ql2, anticorps C1QL2

Sujet:

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.

ID gène: 165257