ALG11 Antikörper (C-Term)
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- Target Alle ALG11 Antikörper anzeigen
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
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Bindungsspezifität
- C-Term
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Reaktivität
- Human, Maus, Ratte, Kaninchen, Pferd, Hund, Rind (Kuh), Meerschweinchen, Saccharomyces cerevisiae, Zebrafisch (Danio rerio)
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser ALG11 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC)
- Sequenz
- LHTMWNEHFG IGVVECMAAG TIILAHNSGG PKLDIVIPHE GDITGFLAES
- Homologie
- Cow: 92%, Dog: 86%, Guinea Pig: 93%, Horse: 100%, Human: 93%, Mouse: 100%, Rabbit: 86%, Rat: 100%, Yeast: 92%, Zebrafish: 91%
- Produktmerkmale
- This is a rabbit polyclonal antibody against ALG11. It was validated on Western Blot and immunohistochemistry.
- Aufreinigung
- Affinity Purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human ALG11
- Top Product
- Discover our top product ALG11 Primärantikörper
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- Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
- Kommentare
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Antigen size: 492 AA
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- 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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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." in: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).
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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." in: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).
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- Target
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
- Andere Bezeichnung
- ALG11 (ALG11 Produkte)
- Synonyme
- UTP14C antikoerper, CDG1P antikoerper, GT8 antikoerper, RGD1564725 antikoerper, AI849156 antikoerper, AW492253 antikoerper, B230397C21 antikoerper, si:dkey-1h24.5 antikoerper, wu:fj04e04 antikoerper, asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase antikoerper, ALG11, alpha-1,2-mannosyltransferase antikoerper, ALG11, alpha-1,2-mannosyltransferase L homeolog antikoerper, asparagine-linked glycosylation 11 (alpha-1,2-mannosyltransferase) antikoerper, alg11 antikoerper, ALG11 antikoerper, alg11.L antikoerper, Alg11 antikoerper
- Hintergrund
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The function remains unknown.
Alias Symbols: GT8, KIAA0266, CDG1P
Protein Interaction Partner: UBC,
Protein Size: 492 - Molekulargewicht
- 56 kDa
- Gen-ID
- 440138
- NCBI Accession
- NM_001004127, NP_001004127
- UniProt
- Q2TAA5
- Pathways
- SARS-CoV-2 Protein Interaktom
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