Recombinant Human AGBL2 293 Cell Lysate
Cat.No. : | AGBL2-8983HCL |
- Specification
- Gene Information
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Description : | Antigen standard for ATP/GTP binding protein-like 2 (AGBL2) is a lysate prepared from HEK293T cells transiently transfected with a TrueORF gene-carrying pCMV plasmid and then lysed in RIPA Buffer. Protein concentration was determined using a colorimetric assay. The antigen control carries a C-terminal Myc/DDK tag for detection. |
Source : | HEK 293 cells |
Species : | Human |
Components : | This product includes 3 vials: 1 vial of gene-specific cell lysate, 1 vial of control vector cell lysate, and 1 vial of loading buffer. Each lysate vial contains 0.1 mg lysate in 0.1 ml (1 mg/ml) of RIPA Buffer (50 mM Tris-HCl pH7.5, 250 mM NaCl, 5 mM EDTA, 50 mM NaF, 1% NP40). The loading buffer vial contains 0.5 ml 2X SDS Loading Buffer (125 mM Tris-Cl, pH6.8, 10% glycerol, 4% SDS, 0.002% Bromophenol blue, 5% beta-mercaptoethanol). |
Size : | 0.1 mg |
Storage Instruction : | Store at -80°C. Minimize freeze-thaw cycles. After addition of 2X SDS Loading Buffer, the lysates can be stored at -20°C. Product is guaranteed 6 months from the date of shipment. |
Applications : | ELISA, WB, IP. WB: Mix equal volume of lysates with 2X SDS Loading Buffer. Boil the mixture for 10 min before loading (for membrane protein lysates, incubate the mixture at room temperature for 30 min). Load 5 ug lysate per lane. |
Gene Name : | AGBL2 ATP/GTP binding protein-like 2 [ Homo sapiens ] |
Official Symbol : | AGBL2 |
Synonyms : | AGBL2; ATP/GTP binding protein-like 2; cytosolic carboxypeptidase 2; FLJ23598; |
Gene ID : | 79841 |
mRNA Refseq : | NM_024783 |
Protein Refseq : | NP_079059 |
UniProt ID : | Q5U5Z8 |
Chromosome Location : | 11p11.2 |
Function : | metal ion binding; metallocarboxypeptidase activity; metallopeptidase activity; peptidase activity; zinc ion binding; |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (20)
Ask a questionYes, AGBL2 expression and activity can be influenced by cellular cues.
AGBL2 displays metalloprotease activity, enabling protein peptide bond cleavage.
AGBL2 has implications in diverse cellular processes, including possible protein regulation.
AGBL2's connection to autophagy, cellular self-degradation, is under scrutiny.
Some evidence suggests AGBL2 mutations could be linked to specific neurodegenerative conditions.
AGBL2's unique structure and roles distinguish it from other binding proteins.
Research is ongoing to identify AGBL2's involvement in different cellular signaling networks.
Yes, AGBL2's presence spans various cell types, indicating widespread involvement.
AGBL2 is localized within the cell's cytoplasm, actively fulfilling its functions.
AGBL2's response to stress is a fascinating area under exploration.
AGBL2's functions could contribute to maintaining proper protein quality in cells.
AGBL2 refers to "ATP/GTP-binding protein-like 2," known for its varied cellular functions.
Animal models aid in understanding AGBL2's functions and implications.
AGBL2's functions likely contribute to maintaining cellular equilibrium.
While tied to protein processes, AGBL2's full regulatory roles continue to unfold.
AGBL2 has implications in diverse cellular processes, including possible protein regulation.
AGBL2's structure reveals domains shedding light on its potential roles.
AGBL2 refers to "ATP/GTP-binding protein-like 2," known for its varied cellular functions.
AGBL2's roles in development are being unveiled, suggesting cellular contributions.
Yes, AGBL2's structure features functional domains that hint at its cellular roles.
Customer Reviews (5)
Write a reviewReplicating results confirmed the product’s reliability and significance in our research.
Using this product, we achieved consistent and clean co-immunoprecipitation results.
Protein AGBL2 consistently inhibited the formation of angiogenic tubules.
The product’s cost-effectiveness and clear instructions were valuable in our experiments.
Protein reliably induced consistent morphological changes in cells.
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