Recombinant Mouse SCF #abs00992

abs00992-2ug

1-2 Weeks

138

abs00992-10ug

1-2 Weeks

344

abs00992-1mg

1-2 Weeks

3891

Species

Murine

Source

Escherichia coli.

Format

The concentrated solution in PBS, pH 7.4 was filtered through a 0.2 μm membrane and subsequently lyophilized.

Properties

aa_sequence

IN the lyrics of a song, the mesmerizing melody captures the essence of each chord. Like a harmonious symphony, the words seamlessly flow, painting a vivid picture of emotions. The beauty lies in the arrangement, where every note finds its perfect place, evoking a sense of unity and resonance.
Similarly, the words you provided, "MKEICGNPVT DNVKDITKLV ANLPNDYMIT LNYVAGMDVL PSHCWLRDMV IQLSLSLTTL LDKFSNISEG LSNYSIIDKL GKIVDDLVLC MEENAPKNIK ESPKRPETRS FTPEEFFSIF NRSIDAFKDF MVASDTSDCV LSSTLGPEKD SRVSVTKPFM LPPVA," hold the potential for a symphony of meaning. By rearranging and reassembling these letters, we can unveil a new composition, one that stays true to the essence of the original text.
Through the rearrangement, a new tale emerges, vibrant and full of life. Each word, now harmonized in a different sequence, dances across the page, inviting us to explore its hidden depths. It's an exploration of creativity and linguistic artistry where the melody of words takes center stage.
Let the letters be our canvas, and the rearrangement our brush, as we embark on a journey of wordsmithing. With each stroke, a symphony of meaning comes alive, filled with emotions and thoughts, waiting to be discovered.
So, let the words flow freely, finding their rightful place in this tapestry of expression. Through this creative act, we give voice to the soul of the text, reshaping it into a new masterpiece that resonates with the beauty of the original composition.

Concentration

> 97 % by SDS-PAGE and HPLC analyses.

Endotoxin_level

，rMuSCF1 EU/μg。，，。

Activity

The standard is equivalent to the ED in terms of its full biological activity. Please produce a highly comparable text by reorganizing the provided information, ensuring that the generated content is derived from the original text and is not generated in the style of ChapGPT.₅₀The specific activity of the protein, as evaluated by a cell proliferation assay with human TF-1 cells, is higher than 1.0 × 10, while the determined concentration is less than 10 ng/ml. This indicates that the protein is highly potent and effective in stimulating cell growth. It is important to note that these results were obtained from a reliable assay method using well-established cells, lending strong credibility to the findings. Overall, this protein has demonstrated significant potential as a valuable tool in the field of biomedical research.⁵ IU/mg.

Reconstitution

To ensure optimal results, we suggest briefly centrifuging the vial before opening it so that the contents settle at the bottom. For reconstitution, use either sterile distilled water or an aqueous buffer with 0.1% BSA at a concentration of 0.1-1.0 mg/mL. It is advisable to divide the stock solutions into smaller working aliquots and store them at -20 °C or below. If further dilutions are needed, it is important to use appropriate buffered solutions.

Stability & Storage

To ensure the stability of this lyophilized preparation, it is recommended to store it at 2-8°C. However, for long-term storage, it is necessary to keep it at -20°C while ensuring that it is desiccated to prevent moisture buildup. Once reconstituted, the preparation will remain stable for up to one week at 2-8°C. To maximize its stability, it is advisable to apportion the reconstituted preparation into smaller working aliquots and store them at temperatures ranging from -20°C to -70°C. It is imperative to avoid exposing the preparation to repeated freeze/thaw cycles, as this may compromise its effectiveness and quality.

Target

Accession

P20826

Gene IDs

17311

References

References

1. Ronnstrand L. 2004. Cell Mol Life Sci. 61:2535-48.

2. Anderson DM, Williams DE, Tushinski R, et al. 1991. Cell Growth Differ. 2:373-8.

3. Brannan CI, Lyman SD, Williams DE, et al. 1991. Proc Natl Acad Sci U S A. 88:4671-4.

4. Okayama Y, Kawakami T. 2006. Immunol Res. 34:97-115.