Thermo Fisher Scientific PEX7 Polyclonal Antibody
Human PEX7 단백질을 인식하는 Rabbit Polyclonal 항체로, IHC(P)에서 1:20~1:50 희석 비율로 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS(40% glycerol) 버퍼에 보관. 단기 4°C, 장기 -20°C 보관 권장.
- 카탈로그번호
- PA561908
- 판매단위
- pk
카탈로그
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Applications
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:20–1:50
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human PEX7. Recombinant protein control fragment (Product # RP-94691) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.05 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_2645415 |
Product Specific Information
Immunogen sequence:
MSAVCGGAAR MLRTPGRHGY AAEFSPYLPG RLACATAQHY GIAGCGTLLI LDPDEAGLRL FRSFDWNDGL FDVTWSENNE HVLITCSGD
- Highest antigen sequence identity to orthologs:
- Mouse: 81%
- Rat: 80%
Target Information
This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2).
Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function.
There are at least 14 complementation groups for PBDs, with more than one phenotype observed in specific groups.
Although clinical features vary, all PBD patient cells exhibit defects in import of one or more classes of peroxisomal matrix proteins.
Defects in this gene are associated with:
- PBD complementation group 11 (PBD-CG11)
- Rhizomelic chondrodysplasia punctata type 1 (RCDP1)
- Refsum disease (RD)
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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