ERManI Antibody (3C2) - Azide and BSA Free Summary
| Immunogen |
Full length human recombinant ERManI [Swiss-Prot# Q9UKM7] |
| Isotype |
IgG1 Kappa |
| Clonality |
Monoclonal |
| Host |
Mouse |
| Gene |
MAN1B1 |
| Purity |
Protein G purified |
| Innovator's Reward |
Test in a species/application not listed above to receive a full credit towards a future purchase. |
Applications/Dilutions
| Dilutions |
- ELISA 1:1000
- Immunocytochemistry/ Immunofluorescence 1:100
- Immunohistochemistry 1:200
- Immunohistochemistry-Paraffin 1:200
- Immunoprecipitation 1:10-1:100
- Knockout Validated reported in scientific literature (PMID 26205822)
- Western Blot 1:500-1:1000
|
| Application Notes |
In ICC/IF, endoplasmic reticulum membrane staining was observed in HeLa cells. In Western Blot, a band is seen ~90 kDa representing ERManI. In IHC-P, staining was observed in the endoplasmic reticulum of human breast cancer tissue. Prior to immunostaining paraffin tissues, antigen retrieval with sodium citrate buffer (pH 6.0) is recommended. |
Reactivity Notes
Does not react with mouse.
Packaging, Storage & Formulations
| Storage |
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles. |
| Buffer |
Tris-Glycine (pH 7.5), 0.15M NaCl |
| Preservative |
No Preservative |
| Concentration |
1 mg/ml |
| Purity |
Protein G purified |
Alternate Names for ERManI Antibody (3C2) - Azide and BSA Free
Background
ERManI, also known as endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase or MAN1B1, is a putative ER resident mannosidase that plays a rate-limiting role in generating a signal that targets misfolded N-linked glycoproteins for ER-associated degradation (ERAD). ERManI codes for an enzyme that converts Man9GlcNAc to Man8GlcNAc isomer B during N-glycan biosynthesis. It also facilitates the trimming of Man5-6GlcNAc2 in the endoplasmic reticulum associated degradation pathway. Multiple transcript variants of ERManI can result from alternative splicing, and a related pseudogene can be found on chromosome 11. Research has found that mutations on the ERManI gene can result in autosomal-recessive intellectual disabilities and developmental delays (PMID: 21763484). ERManI is predominately localized to the Golgi and endoplasmic reticulum.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are
guaranteed for 1 year from date of receipt.
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