C1QL2 Antikörper (Alexa Fluor 647)

Produktnummer ABIN1404702

Produktdetails anti-C1QL2 Antikörper (Alexa Fluor 647)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C1QL2 Antikörper ist konjugiert mit Alexa Fluor 647

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu C1QL2

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

Andere Bezeichnung: C1QTNF10 (C1QL2 Produkte)

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

Hintergrund:

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.

Gen-ID: 165257