Arylsulfatase E anticorps (Middle Region)
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- Antigène Voir toutes Arylsulfatase E (ARSE) Anticorps
- Arylsulfatase E (ARSE)
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Épitope
- Middle Region
- Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Arylsulfatase E est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS
- Homologie
- Human: 100%
- Attributs du produit
- This is a rabbit polyclonal antibody against ARSE. It was validated on Western Blot using a cell lysate as a positive control.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human ARSE
- Top Product
- Discover our top product ARSE Anticorps primaire
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- Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
- Commentaires
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Antigen size: 589 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Antigène
- Arylsulfatase E (ARSE)
- Autre désignation
- ARSE (ARSE Produits)
- Synonymes
- anticorps ASE, anticorps CDPX, anticorps CDPX1, anticorps CDPXR, anticorps ARSE, anticorps MGC155058, anticorps arylsulfatase E (chondrodysplasia punctata 1), anticorps arylsulfatase E, anticorps ARSE, anticorps Arse
- Sujet
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Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-170 AC005295.1 87561-87730 c 171-744 AK223183.1 1-574 745-2036 AK223199.1 542-1833 2037-2220 AW779826.1 1-184 c
Alias Symbols: CDPX, CDPX1, CDPXR, MGC163310, ASE
Protein Interaction Partner: COQ6, TMEM259, TNK2, NDN,
Protein Size: 589 - Poids moléculaire
- 62 kDa
- ID gène
- 415
- NCBI Accession
- NM_000047, NP_000038
- UniProt
- P51690
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