LOX anticorps (AA 22-168)
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- Antigène Voir toutes LOX Anticorps
- LOX (Lysyl Oxidase (LOX))
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Épitope
- AA 22-168
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp LOX est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (IF)
- Attributs du produit
- Homo sapiens lysyl oxidase (LOX), transcript variant 1
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogène
- Human recombinant protein fragment corresponding to amino acids 22-168 of human LOX (NP_002308) produced in HEK293T cell.
- Clone
- 10D11
- Isotype
- IgG1
- Top Product
- Discover our top product LOX Anticorps primaire
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- Indications d'application
- WB 1:1000, IHC 1:150, IF 1:100, FLOW 1:100,
- Commentaires
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The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS ( pH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
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- Antigène
- LOX (Lysyl Oxidase (LOX))
- Autre désignation
- LOX (LOX Produits)
- Synonymes
- anticorps LOX, anticorps Xlox, anticorps MGC146507, anticorps lox, anticorps zgc:77447, anticorps AI893619, anticorps TSC-160, anticorps H-rev142, anticorps Rrg1, anticorps lysyl oxidase, anticorps lysyl oxidase a, anticorps lysyl oxidase L homeolog, anticorps LOX, anticorps lox, anticorps loxa, anticorps lox.L, anticorps Lox
- Sujet
- The protein encoded by this gene is an extracellular copper enzyme that initiates the crosslinking of collagens and elastin. The enzyme catalyzes oxidative deamination of the epsilon-amino group in certain lysine and hydroxylysine residues of collagens and lysine residues of elastin. In addition to crosslinking extracellular matrix proteins, the encoded protein may have a role in tumor suppression. Defects in this gene are a cause of autosomal recessive cutis laxa type I (CL type I). Two transcript variants encoding different isoforms have been found for this gene.
- Poids moléculaire
- 46.8 kDa
- ID gène
- 4015
- NCBI Accession
- NM_002317
- HGNC
- 4015
- Pathways
- SARS-CoV-2 Protein Interactome
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