Thermo Fisher Scientific BRP44L Polyclonal Antibody
BRP44L 단백질을 인식하는 Rabbit Polyclonal 항체로, IHC(P)에서 1:50~1:200 희석 비율로 사용 가능. 인간, 마우스, 랫트 반응성. 항원 친화 크로마토그래피로 정제되었으며, 1 mg/mL 액상 형태. 연구용으로만 사용 가능.
- 판매단위
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Applications
- Immunohistochemistry (Paraffin) (IHC (P)): 1:50–1:200
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide corresponding to amino acids 20–70 of human BRP44L |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7.2, with 50% 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_2553525 |
Product Specific Information
This antibody detects endogenous BRP44L protein at a molecular weight of approximately 12 kDa.
Purity is greater than 95% as determined by SDS-PAGE.
Target Information
BRP44L (brain protein 44-like protein), also known as HSPC040 or CGI-129, is a 109 amino acid mitochondrial protein belonging to the UPF0041 family. The gene encoding BRP44L is located on human chromosome 6, which contains around 1,200 genes across 170 million base pairs.
Chromosome 6 is associated with various diseases and genetic conditions, including:
- Early onset intestinal cancer (q arm deletion)
- Porphyria cutanea tarda (HFE gene mutation)
- Parkinson’s disease (PARK2 gene)
- Rheumatic diseases (MHC complex genes)
- Stickler syndrome, 21-hydroxylase deficiency, maple syrup urine disease, and bipolar disorder susceptibility loci
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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