Thermo Fisher Scientific WBSCR27 Polyclonal Antibody
Human WBSCR27 단백질을 인식하는 Rabbit Polyclonal Antibody로 Western blot과 Immunocytochemistry에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보존됩니다. 연구용으로만 사용 가능합니다.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 0.04–0.4 µg/mL |
| Immunocytochemistry (ICC/IF) | 0.25–2 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human WBSCR27 (target family: METTL27, UniProt ID: Q8N6F8-1, antigen range: 165–238, antigen length: 245) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.2 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_2649540 |
Product Specific Information
Immunogen sequence:
LTTRTNSSNL QYKEALEATL DRLEQAGMWE GLVAWPVDRL WTAGSWLPPS WRWYPASLPR MASSPALSTC TESG
Sequence identity:
- Mouse: 39%
- Rat: 41%
Target Information
This gene encodes a protein belonging to the ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22–q11.23.
(Provided by RefSeq, Jul 2008)
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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