C1QL2 anticorps (AA 200-280)
Aperçu rapide pour C1QL2 anticorps (AA 200-280) (ABIN7213882)
Antigène
Voir toutes C1QL2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 200-280
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Fonction
- C1qL2 Polyclonal Antibody
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Specificité
- C1qL2 Polyclonal Antibody detects endogenous levels of C1qL2 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogène
- Synthesized peptide derived from the C-terminal region of human C1qL2 at AA range: 200-280
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
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Commentaires
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- C1QL2 (Complement Component 1, Q Subcomponent-Like 2 (C1QL2))
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Autre désignation
- C1qL2
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Sujet
- Rabbit Anti-C1qL2 Polyclonal Antibody,C1QL2, Complement C1q-like protein 2,C1qL2 (complement C1q-like protein 2), 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, Alström syndrome, is due to mutations in the ALMS1 gene.,Complement C1q-like protein 2
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Poids moléculaire
- observerd band 32-36kDa
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ID gène
- 165257
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UniProt
- Q7Z5L3
Antigène
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