Human Serine Peptidase Inhibitor Kazal Type 1 (SPINK1) Protein

234€ (10 µg)
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935106861
info@markelab.com
name
Human Serine Peptidase Inhibitor Kazal Type 1 (SPINK1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx069039
tested applications
WB, SDS-PAGE
Description
Mouse Serine Peptidase Inhibitor Kazal Type 1 (SPINK1) is a recombinant Human protein produced in a Prokaryotic expression system (E. coli).
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Proteins and Peptides |
| Immunogen Target | Serine Peptidase Inhibitor Kazal Type 1 (SPINK1) |
| Host | E. coli |
| Origin | Human |
| Conjugation | Unconjugated |
| Observed MW | Molecular Weight: Calculated MW: 38.3 kDa Concentration: Prior to lyophilization: 200 µg/ml Sequence Fragment: Leu26-Pro78 Tag: N-terminal His tag and GST tag |
| Expression | Recombinant |
| Purity | > 95% |
| Size 1 | 10 µg |
| Size 2 | 50 µg |
| Size 3 | 100 µg |
| Size 4 | 200 µg |
| Size 5 | 500 µg |
| Form | Lyophilized To keep the original salt concentration, we recommend reconstituting to the original concentration prior to lyophilization (see Concentration) in ddH2O. If a lower concentration is required, dilute in PBS, pH 7.4. If a higher concentration is required, the product can be reconstituted directly in PBS, pH 7.4, though please note that this will change the overall salt concentration. The stock concentration should be between 0.1-1.0 mg/ml. Do not vortex. |
| Tested Applications | WB, SDS-PAGE |
| Buffer | Prior to lyophilization: PBS, pH 7.4, containing 0.01% Sarcosyl, 1 mM DTT, 5% Trehalose and Proclin-300. |
| Availability | Shipped within 5-7 working days. |
| Storage | Store at 2-8 °C for up to one month. Store at -80 °C for up to one year. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P00995 |
| Gene ID | 6690 |
| OMIM | 167790 |
| Background | Protein SPINK1 |
| Status | RUO |
| Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
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