Thermo Fisher Scientific NUP210L Polyclonal Antibody
Human NUP210L 단백질에 특이적인 Rabbit Polyclonal Antibody로, IHC(P)에서 1:2,500~1:5,000 희석으로 검증됨. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관. 연구용으로 적합하며 인간 NUP210L 단백질 검출에 사용.
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Applications
Immunohistochemistry (Paraffin) [IHC (P)]
- Tested Dilution: 1:2,500–1:5,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human NUP210L (Control fragment: Product #RP-104077) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS (pH 7.2) with 40% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | 4°C (short term), -20°C (long term), avoid freeze/thaw cycles |
| Shipping Conditions | Wet ice |
| RRID | AB_2644897 |
Product Specific Information
Immunogen sequence:
YVCIIKVRPQ SEELLQALSV ADTSVYGWAT LVSERSKNGM QRILIPFIPA FYINQSELVL SHKQDIGEIR VLGVDRVLRK LE
Antigen sequence identity:
- Mouse: 78%
- Rat: 78%
Target Information
Nup210L (nuclear pore membrane glycoprotein 210-like) is a 1,888 amino acid single-pass membrane protein belonging to the NUP210 family.
The NUP210L gene spans approximately 162,432 bases and maps to human chromosome 1q21.3.
Chromosome 1 is the largest human chromosome, comprising about 260 million base pairs and approximately 3,000 genes.
Several diseases are associated with chromosome 1, including Hutchinson-Gilford progeria (LMNA gene), familial adenomatous polyposis (MUTYH gene), Stickler syndrome, Parkinson’s disease, Gaucher disease, and Usher syndrome.
For Research Use Only.
Not for use in diagnostic procedures. Not for resale without express authorization.
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