Universal Pipette Tips
Disposable pipette tips designed to fit single and multichannel pipettes from most manufacturers; offer acceptable performance compared to pipette specific tips and can be used with a variety of pipette models.
Single-use universal pipette tips are designed for compatibility with most mechanical and electronic single and multichannel pipettors.
Universal pipette tips are available in a range of types, sizes, colors, styles, and packaging configurations and may be designed for specific purposes or tasks.
- Capacity or volume based on the pipettor size
- Filters to reduce contamination and cross-contamination
- Color
- Sterility or autoclavability
- Tip style: beveled, tapered, wide bore, round, flat, or gel-loading
- Length: short or extended
- Purity: metal-free or DNase-, RNase-, ATP-, Bioburden-, PCR inhibitor-, endotoxin-, or pyrogen-free for genomic and biologic applications
- Surface treatments to reduce retention
- Packaging options to help facilitate re-stocking or eliminate waste
ABclonal Technology β-TrCP/BTRC Rabbit pAb
This gene encodes an F-box protein, part of the F-box protein family, characterized by a 40 amino acid F-box motif. F-box proteins are subunits of the SCF (SKP1-cullin-F-box) complex, involved in phosphorylation-dependent ubiquitination. The F-box proteins are classified into three classes: Fbws, Fbls, and Fbxs. The protein encoded by this gene belongs to the Fbws class, containing both an F-box and multiple WD-40 repeats. It mediates CD4 degradation through interaction with HIV-1 Vpu and ubiquitinates phosphorylated NFKBIA, targeting it for degradation and activating nuclear factor kappa-B. Alternative splicing results in multiple transcript variants, and a related pseudogene exists on chromosome 6.
ABclonal Technology CLDN2 Rabbit pAb
This gene product belongs to the claudin protein family whose members have been identified as major integral membrane proteins localized exclusively at tight junctions. Claudins are expressed in an organ-specific manner and regulate tissue-specific physiologic properties of tight junctions. This protein is expressed in the intestine. Alternatively spliced transcript variants with different 5 untranslated region have been found for this gene.
ABclonal Technology FREM2 Rabbit pAb
This gene encodes an integral membrane protein containing numerous CSPG (chondroitin sulfate proteoglycan element) repeats and Calx-beta domains. The encoded protein localizes to the basement membrane, forming a ternary complex that plays a role in epidermal-dermal interactions. This protein is important for the integrity of skin and renal epithelia. Mutations in this gene are associated with Fraser syndrome.
ABclonal Technology CHMP7 Rabbit pAb
Involved in several processes, including late endosome to vacuole transport, midbody abscission, and mitotic nuclear division. Located in cytosol, nuclear envelope, and nucleoplasm. Part of ESCRT III complex. Colocalizes with chromatin.
ABclonal Technology RNF220 Rabbit pAb
Predicted to enable ubiquitin protein ligase activity. Involved in positive regulation of canonical Wnt signaling pathway. Part of protein-containing complex.
ABclonal Technology FGGY Rabbit pAb
This gene encodes a protein that phosphorylates carbohydrates such as ribulose, ribitol, and L-arabinitol. Genome-wide association studies in some populations have found an association between polymorphisms in this gene and sporadic amyotrophic lateral sclerosis, but studies of other populations have not been able to replicate this association. Alternative splicing results in multiple transcript variants.
ABclonal Technology MIIP Rabbit pAb
This gene encodes a protein that interacts with the oncogene protein insulin-like growth factor binding protein 2 and may function as an inhibitor of cell migration and invasion. This protein also interacts with the cell division protein 20 and may be involved in regulating mitotic progression. This protein may function as a tumor suppressor by inhibiting the growth or certain cancers.
ABclonal Technology ZNF248 Rabbit pAb
Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus.
ABclonal Technology ACMSD Rabbit pAb
The neuronal excitotoxin quinolinate is an intermediate in the de novo synthesis pathway of NAD from tryptophan, and has been implicated in the pathogenesis of several neurodegenerative disorders. Quinolinate is derived from alpha-amino-beta-carboxy-muconate-epsilon-semialdehyde (ACMS). ACMSD (ACMS decarboxylase, EC 4.1.1.45) can divert ACMS to a benign catabolite and thus prevent the accumulation of quinolinate from ACMS.
ABclonal Technology DHRS11 Rabbit pAb
Enables 17-beta-hydroxysteroid dehydrogenase (NADP+) activity, 17-beta-ketosteroid reductase activity, and 3-keto sterol reductase activity. Involved in steroid biosynthetic process. Predicted to be located in extracellular region.
ABclonal Technology TRPV6 Rabbit pAb
This gene encodes a member of a family of multipass membrane proteins that functions as calcium channels. The encoded protein contains N-terminal ankyrin repeats, which are required for channel assembly and regulation. Translation initiation for this protein occurs at a non-AUG start codon that is decoded as methionine. This gene is situated next to a closely related gene for transient receptor potential cation channel subfamily V member 5 (TRPV5). This locus has experienced positive selection in non-African populations, resulting in several non-synonymous codon differences among individuals of different genetic backgrounds.
ABclonal Technology NDUFAF4 Rabbit pAb
NADHubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene are a cause of mitochondrial complex I deficiency.
ABclonal Technology KIF5B Rabbit pAb
Enables identical protein binding activity, microtubule binding activity, and microtubule motor activity. Involved in several processes, including lysosome localization, natural killer cell mediated cytotoxicity, and positive regulation of protein localization to plasma membrane. Located in centriolar satellite, cytosol, and vesicle.
Alkali Scientific Gel Loading Tips, 200uL 83mm Length, Round bore opening, 960 tips/Case, Sterile
Gel Loading Tips, 200 µL, 83 mm Length are designed for precise and controlled sample loading in electrophoresis applications. The extra long 83 mm profile provides easy access to deep or narrow gel wells, while the round bore opening ensures smooth flow and minimizes bubble formation for accurate dispensing. Precision molded for consistent performance, these tips are ideal for DNA, RNA, and protein gel loading workflows. Packaged in 2 racks of 96 tips per inner pack, with 5 inner packs per case, totaling 960 tips per case. This high throughput packaging supports efficient laboratory use. Key Features: 200 µL volume capacity for large gel loading applications, 83 mm extra long length for easy access to deep or narrow wells, round bore opening for smooth dispensing, reduces bubble formation and sample loss, non filtered design for electrophoresis workflows, precision molded for consistent results, compatible with standard micropipettes.
ABclonal Technology Adenosine Deaminase (ADA) Rabbit pAb
This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine in the purine catabolic pathway. Various mutations have been described for this gene and have been linked to human diseases related to impaired immune function such as severe combined immunodeficiency disease (SCID) which is the result of a deficiency in the ADA enzyme. In ADA-deficient individuals there is a marked depletion of T, B, and NK lymphocytes, and consequently, a lack of both humoral and cellular immunity. Conversely, elevated levels of this enzyme are associated with congenital hemolytic anemia.