Thermo Fisher Scientific CLN5 Polyclonal Antibody
인간 CLN5 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 IHC(P)에서 검증됨. 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공. 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 0.04–0.4 µg/mL
- Publications: References
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:500–1:1,000
- Publications: References
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human CLN5. Recombinant protein control fragment (Product #RP-97938). |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.4 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage buffer | PBS, pH 7.2, with 40% glycerol |
| Contains | 0.02% sodium azide |
| Storage conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping conditions | Wet ice |
| RRID | AB_2639894 |
Product Specific Information
Immunogen sequence:
TLTGKNYTME WYELFQLGNC TFPHLRPEMD APFWCNQGAA CFFEGIDDVH WKENGTLVQV ATISGNMFNQ MAKWVKQDNE TGIYYETWNV KASPEK
Antigen sequence identity:
- Mouse: 83%
- Rat: 85%
Target Information
This gene is one of eight associated with neuronal ceroid lipofuscinoses (NCL), also known as Batten disease. NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes involved are likely to encode proteins responsible for degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.
[Provided by RefSeq, Oct 2008]
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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