
Thermo Fisher Scientific HAX1 Polyclonal Antibody
HAX1 단백질을 인식하는 Thermo Fisher Scientific의 토끼 다클론 항체. Western blot, ELISA, IP에 사용 가능하며 인간, 생쥐, 랫드 등 다양한 종에 반응. 친화 크로마토그래피로 정제된 액상 항체로, -20°C에서 보관. 연구용 전용 제품.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:2,000 |
| ELISA | 1:10,000 |
| Immunoprecipitation (IP) | 1 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Chicken, Human, Mouse, Non-human primate, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Anti-HAX1 affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to the internal region of human HAX1 protein. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1.78 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | 0.02M potassium phosphate, pH 7.2, with 30% glycerol, 0.15M NaCl |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
- Store vial at -20°C prior to opening.
- Aliquot contents and freeze at -20°C or below for extended storage.
- Avoid repeated freeze/thaw cycles.
- Centrifuge product if not completely clear after standing at room temperature.
- Stable for several weeks at 4°C as an undiluted liquid.
- Dilute only prior to immediate use.
- Anti-HAX1 was affinity purified from monospecific antiserum by immunoaffinity chromatography.
- BLAST analysis suggests cross-reactivity with human, rat, and mouse based on 100% sequence homology.
- Cross-reactivity with HAX1 from other sources has not been determined.
Target Information
The HAX1 gene encodes a protein associated with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It interacts with the polycystic kidney disease 2 gene product and the F-actin-binding protein cortactin. Initially thought to be localized in mitochondria, it is now known to localize in the cell body. Mutations in this gene cause autosomal recessive severe congenital neutropenia (Kostmann disease). Two transcript variants encoding different isoforms have been identified.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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