GNL1 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- 产品详情
- 实验流程
- 背景知识
Application ![]()
| WB, E |
---|---|
Primary Accession | P36915 |
Other Accession | Q4R8D2, NP_005266.2 |
Reactivity | Human |
Predicted | Monkey |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 68661 Da |
Antigen Region | 240-266 aa |
Gene ID | 2794 |
---|---|
Other Names | Guanine nucleotide-binding protein-like 1, GTP-binding protein HSR1, GNL1, HSR1 |
Target/Specificity | This GNL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 240-266 amino acids from the Central region of human GNL1. |
Dilution | WB~~1:1000 E~~Use at an assay dependent concentration. |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | GNL1 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | GNL1 |
---|---|
Synonyms | HSR1 |
Function | Possible regulatory or functional link with the histocompatibility cluster. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
The GNL1 gene, identified in the human major histocompatibility complex class I region, shows a high degree of similarity with its mouse counterpart. The GNL1 gene is located less than 2 kb centromeric to HLA-E, in the same transcriptional orientation. GNL1 is telomeric to HLA-B and HLA-C. [provided by RefSeq].
REFERENCES
Barcellos, L.F., et al. PLoS Genet. 5 (10), E1000696 (2009) :
Paladini, F., et al. Arthritis Res. Ther. 11 (6), R171 (2009) :
Matsuoka, S., et al. Science 316(5828):1160-1166(2007)
Matsuoka, S., et al. Science 316(5828):1160-1166(2007)
Olsen, J.V., et al. Cell 127(3):635-648(2006)

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