NUP210L Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA565465-Each-of-1 | In Stock | ₹ 48,905.50 |
PIPA565465 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 48,905.50
GST (18%): ₹ 8,802.99
Total Price: ₹ 57,708.49
Antigen
NUP210L
Classification
Polyclonal
Conjugate
Unconjugated
Gene
NUP210L
Gene Alias
Nuclear pore membrane glycoprotein 210-like; nuclear pore membrane glycoprotein 210-like (LOC91181); Nucleoporin 210 kDa-like; nucleoporin 210 like; nucleoporin 210kDa like; nucleoporin 210kDa-like; nucleoporin 210-like; nucleoporin Nup210-like; NUP210L; RGD1310250
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
91181
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunocytochemistry
Concentration
0.05 mg/mL
Formulation
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
Gene Accession No.
Q5VU65
Gene Symbols
NUP210L
Immunogen
Recombinant Human NUP210L
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: PINSQLKLHTN REGAAFVSSR VLKCFPNSSV IEEDGEGLLK AGSIAGTAVL EVTSIEPFGV NQTTITGVQV APVTYLRVSS QPKLYTAQGR TLSAFPLGMS LTFTVQFYNS IGEKFHTHNT QLYLALN Highest antigen sequence identity to the following orthologs - mouse 91%, rat 91%
- Nup210L (nuclear pore membrane glycoprotein 210-like) is a 1,888 amino acid single-pass membrane protein that belongs to the NUP210 family
- The gene that encodes Nup210L consists of approximately 162,432 bases and maps to human chromosome 1q21.3
- Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome
- There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1
- Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A
- When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs
- The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis
- Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.