LMAN1 antibody (AA 270-470)
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- Target See all LMAN1 Antibodies
- LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))
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Binding Specificity
- AA 270-470
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Reactivity
- Human
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Host
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Chicken
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Clonality
- Polyclonal
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Conjugate
- This LMAN1 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purification
- Immunoaffinity Purified
- Top Product
- Discover our top product LMAN1 Primary Antibody
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- Application Notes
- ERGIC-53 protein antibody can be used for the detection of ERGIC-53 protein by Western Blot.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- Phosphate-Buffered Saline. No preservatives added.
- Preservative
- Without preservative
- Handling Advice
- As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
- Storage
- 4 °C/-20 °C
- Storage Comment
- LMAN1 antibody can be stored at 4 °C for short term (weeks). Long term storage should be at -20 °C.
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- Target
- LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))
- Alternative Name
- LMAN1 (LMAN1 Products)
- Synonyms
- ERGIC-53 antibody, ERGIC53 antibody, F5F8D antibody, FMFD1 antibody, MCFD1 antibody, MR60 antibody, gp58 antibody, 2610020P13Rik antibody, AI326273 antibody, AU043785 antibody, C730041J05 antibody, P58 antibody, p58 antibody, LMAN1 antibody, cpx-iii antibody, cpxiii antibody, lman1 antibody, wu:fc54c09 antibody, wu:fi36e01 antibody, Xp58 antibody, lman1-a antibody, lectin, mannose binding 1 antibody, lectin, mannose-binding, 1 antibody, complexin 3 antibody, lectin, mannose binding 1 S homeolog antibody, LMAN1 antibody, Lman1 antibody, cplx3 antibody, lman1 antibody, lman1.S antibody
- Background
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FUNCTION: Mannose-specific lectin. May recognize sugar residues of glycoproteins, glycolipids, or glycosylphosphatidyl inositol anchors and may be involved in the sorting or recycling of proteins, lipids, or both. The LMAN1-MCFD2 complex forms a specific cargo receptor for the ER-to-Golgi transport of selected proteins.
DISEASE: Defects in LMAN1 are a cause of factor V and factor VIII combined deficiency (F5F8D) [MIM:227300], also known as multiple coagulation factor deficiency I (MCFD1). F5F8D is an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins. Affected patients present with a moderate bleeding tendency and have factor V and factor VIII levels in the range of 5-30 % of normal. - Molecular Weight
- 57.5 kDa (calculated)
- Gene ID
- 3998
- NCBI Accession
- NP_005561
- UniProt
- P49257
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