HOP Protein

What it means: Target is the identity of the recombinant protein you’re purchasing. The target listed on this page is HOP.

How to interpret here: Use HOP as your primary “construct match” checkpoint—confirm it is the exact protein/isoform you need for your antibody validation, binding study, or assay standard. The sequence origin is Human, which matters when antibodies or receptors are species‑specific. The expression system is E. coli, which can affect folding and post‑translational modifications. Choose this when target + origin + construct match your application; consider a different construct if you need a specific domain, tag‑free format, or native PTMs.

Why it matters for buying:

• Binding and specificity: Different isoforms, fragments, or closely related family members can change antibody/ligand binding.
• Functional relevance: A fragment may be ideal for epitope mapping but may not reproduce full‑length conformation or activity.
• Reproducibility: Documented construct details (origin, length/region, expression system) reduce surprises between experiments and batches.

Helpful selection notes for this listing:

• Synonyms: HOP, HSP co chaperone, STIP1, Stress-induced-phosphoprotein 1, Hsp70/Hsp90-organizing.

Practical guidance:

• Confirm your epitope/domain: If you have an antibody epitope map or domain requirement, verify it is present in the construct (length/region).
• Plan controls: Include an unrelated protein control (and, when possible, a known‑binding antibody/ligand) to detect non‑specific binding.
• Pilot before scaling: For critical assays, test a small amount first to confirm binding/activity under your exact buffer and immobilization conditions.

What to watch out for:

• PTM‑dependent binding: If your antibody/ligand requires glycosylation or native folding, confirm the expression system supports it.
• Tag or fusion effects: If a tag is present, it can change binding or introduce background—use tag controls when needed.
• Assay standard fit: For quantitative standards, confirm the standard curve behavior in your matrix and avoid relying on concentration claims without lot documentation.

What it means: Species refers to the organism the protein sequence is derived from. The value on this page is Human.

How to interpret here: Use Human to decide if this protein matches the biology you’re studying and the reagents you plan to use. This listing is for HOP derived from Human. Choose this when your antibody/ligand is expected to recognize this origin; validate when using it to test cross‑reactivity across species.

Why it matters for buying:

• Epitope differences: Small sequence changes across species can dramatically alter antibody binding.
• Interpretation of binding: A “negative” result with one species protein may reflect sequence mismatch rather than true lack of binding.
• Translational relevance: If your end goal is human biology, using the human origin protein reduces ambiguity.

Practical guidance:

• Check reagent docs: Compare the immunogen/epitope or binding region in your antibody datasheet against the species shown here.
• Cross‑species panels: For cross‑reactivity work, test multiple ortholog proteins under identical conditions with proper controls.
• Record construct details: Include species + length/region + expression system in your methods for reproducibility.

What to watch out for:

• Species vs expression host: Species here describes sequence origin, not the expression host (see Expression System).
• Variant coverage: If sequence variants/isoforms matter (pathogens or polymorphic proteins), confirm the exact construct details in the datasheet.

What it means: Expression System is the host used to produce the recombinant protein. The expression system listed here is E. coli.

How to interpret here: Use E. coli to anticipate folding and post‑translational modifications (PTMs), and to judge whether the protein will behave “native‑like” in your assay. Bacterial expression typically lacks mammalian glycosylation and some native PTMs—this can matter for PTM‑dependent antibodies or receptor binding. For HOP, choose the expression host that best matches your question (native PTMs vs rapid bacterial production). Choose this when the host is compatible with your binding/functional needs; consider mammalian/insect expression if native conformation/PTMs are critical.

Why it matters for buying:

• PTMs and conformation: Host selection influences glycosylation, disulfide bonding, and folding—key for many epitopes and receptors.
• Impurity profile: Different hosts introduce different impurities; bacterial systems can also carry endotoxin that matters for cell-based work.
• Assay reproducibility: Using the same expression system across studies improves comparability.

Practical guidance:

• Validate early: Confirm binding/activity with your specific antibody/ligand in a small pilot.
• Choose buffers intentionally: Some hosts produce proteins that are more prone to aggregation—follow recommended storage and reconstitution guidance.

What to watch out for:

• Glycosylation-sensitive binding: Lack of glycosylation can reduce binding for certain antibodies and receptors.
• Aggregation: Reconstitute gently and avoid repeated freeze–thaw; aliquot after reconstitution where possible.
• “Activity” assumptions: Host choice can affect activity—confirm activity is provided/validated if you need functional protein.

What it means: Conjugate(s) describes whether this protein is supplied with a modification (a tag or labeling chemistry) that changes how you capture, detect, or handle it. The value shown here is His tag.

How to interpret here: Treat His tag as your workflow selector—choose it based on how you plan to immobilize the protein (capture surfaces, beads), detect it (fluorescence/streptavidin/anti‑tag), and what background/interference you can tolerate. This listing is for HOP (Human origin). Pair this with expression system (E. coli) when folding/PTMs could affect binding. A His tag supports affinity capture/purification (e.g., Ni‑NTA) and can enable oriented immobilization. If the value mentions a protease site (e.g., TEV), it may allow tag removal (confirm in datasheet).

Why it matters for buying:

• Capture strategy: Tags/conjugates enable oriented immobilization (often more reproducible than passive adsorption).
• Detection and background: Added chemistries expand readout options but also add extra binding sites and background risks.
• Workflow compatibility: Your assay (pull‑downs, BLI/SPR, fluorescence readouts) may depend on having the right conjugate.

Practical guidance:

• Plan controls: Include an unrelated protein with the same conjugate (or a tag/dye control) to identify conjugate‑driven background.
• Prefer oriented capture when possible: Biotin/His/other tags can improve reproducibility versus random plate coating.
• Ni‑NTA conditions: Keep chelators (e.g., EDTA) out of capture buffers and control imidazole to maintain binding.

What to watch out for:

• Interference with binding: Tags/conjugates near an epitope can reduce binding—if results look off, compare to a tag‑free construct.
• Non‑specific interactions: Some labels increase stickiness to plastics—use low‑bind tubes and blockers as appropriate.
• Assuming removability: Do not assume a tag can be cleaved unless a protocol is provided.

What it means: Purity describes how clean the protein preparation is (often estimated by SDS‑PAGE or chromatography). The purity stated here is >90%.

How to interpret here: Use >90% to judge whether the preparation is suitable for your assay’s sensitivity and background tolerance. Choose this when the purity level fits your use-case; consider higher purity/low endotoxin options for quantitative standards, kinetics, or cell-based work.

Why it matters for buying:

• Background signal: Impurities can increase non-specific binding in ELISA coating and surface binding assays.
• Lot-to-lot consistency: Higher purity often reduces variability in sensitive applications.
• Biological confounding: Contaminants (including endotoxin) can produce effects unrelated to your target.

Practical guidance:

• Match purity to application: Screening assays may tolerate lower purity; quantitative standards and kinetics benefit from cleaner prep.
• Quick QC: For critical work, verify band size and major species by SDS‑PAGE/Western on arrival.
• Use controls: Include buffer-only and unrelated protein controls to detect non-specific background.

What to watch out for:

• Purity method differences: SDS‑PAGE estimates are not the same as “single molecular species.”
• Aggregates: Purity does not always report aggregation—inspect solubility and consider running non-reducing gels if relevant.
• Cell-based assays: If you see unexpected inflammatory responses, consider endotoxin and validate with controls.