ALG11 antibody (C-Term)
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- Target See all ALG11 Antibodies
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
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Binding Specificity
- C-Term
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Reactivity
- Human, Mouse, Rat, Horse, Rabbit, Dog, Cow, Guinea Pig, Saccharomyces cerevisiae, Zebrafish (Danio rerio)
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This ALG11 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- LHTMWNEHFG IGVVECMAAG TIILAHNSGG PKLDIVIPHE GDITGFLAES
- Predicted Reactivity
- Cow: 92%, Dog: 86%, Guinea Pig: 93%, Horse: 100%, Human: 93%, Mouse: 100%, Rabbit: 86%, Rat: 100%, Yeast: 92%, Zebrafish: 91%
- Characteristics
- This is a rabbit polyclonal antibody against ALG11. It was validated on Western Blot and immunohistochemistry.
- Purification
- 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 Primary Antibody
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- Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
- Comment
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Antigen size: 492 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.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- 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))
- Alternative Name
- ALG11 (ALG11 Products)
- Synonyms
- UTP14C antibody, CDG1P antibody, GT8 antibody, RGD1564725 antibody, AI849156 antibody, AW492253 antibody, B230397C21 antibody, si:dkey-1h24.5 antibody, wu:fj04e04 antibody, asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase antibody, ALG11, alpha-1,2-mannosyltransferase antibody, ALG11, alpha-1,2-mannosyltransferase L homeolog antibody, asparagine-linked glycosylation 11 (alpha-1,2-mannosyltransferase) antibody, alg11 antibody, ALG11 antibody, alg11.L antibody, Alg11 antibody
- Background
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The function remains unknown.
Alias Symbols: GT8, KIAA0266, CDG1P
Protein Interaction Partner: UBC,
Protein Size: 492 - Molecular Weight
- 56 kDa
- Gene ID
- 440138
- NCBI Accession
- NM_001004127, NP_001004127
- UniProt
- Q2TAA5
- Pathways
- SARS-CoV-2 Protein Interactome
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