Recombinant Full Length Sinapis Alba Chlorophyll A-B Binding Protein 1, Chloroplastic(Cab1) Protein, His-Tagged
Cat.No. : | RFL1169SF |
Product Overview : | Recombinant Full Length Sinapis alba Chlorophyll a-b binding protein 1, chloroplastic(CAB1) Protein (P13851) (36-266aa), fused to N-terminal His tag, was expressed in E. coli. |
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Source : | E.coli expression system |
Species : | Sinapis alba (White mustard) (Brassica hirta) |
Tag : | His |
Form : | Lyophilized powder |
Protein length : | Full Length of Mature Protein (36-266) |
AA Sequence : | RKTVKPTGPSGSPWYGSDRVKYLGP FSGEPPSYLTGEFPGDYGWDTAGLS ADPETFARNR ELEVIHCRWAMLGALGCVFPELLAR NGVKFGEAVWFKAGSQIFSEGGLDY LGNPSLVHAQ SILAIWATQVILMGAVEGYRVAGEG PLGEAEDLLYPGGSFDPLGLATDPE AFAELKVKEI KNGRLAMFSMFGFFVQAIVTGKGPL ENLADHLADPVNNNAWAFATNFVPG K |
Purity : | Greater than 90% as determined by SDS-PAGE. |
Applications : | SDS-PAGE |
Notes : | Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week. |
Storage : | Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles. |
Storage Buffer : | Tris/PBS-based buffer, 6% Trehalose, pH 8.0 |
Reconstitution : | We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference. |
Gene Name : | CAB1 |
Synonyms : | CAB1; Chlorophyll a-b binding protein 1, chloroplastic; LHCII type I CAB-1; LHCP |
UniProt ID : | P13851 |
Gene Name : | CAB1 |
Synonyms : | CAB1; Chlorophyll a-b binding protein 1, chloroplastic; LHCII type I CAB-1; LHCP |
UniProt ID : | P13851 |
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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 (7)
Ask a questionPost-translational modifications on CAB1 can be determined using mass spectrometry or specific biochemical assays.
The specific function of CAB1 would need exploration using cellular and molecular assays.
Direct associations of CAB1 with clinical conditions would require patient sample studies, gene expression profiling, and disease-specific research.
Interaction partners for CAB1 might be identified using co-immunoprecipitation, yeast two-hybrid assays, or proteomic databases.
The role of CAB1 in signaling or metabolic processes can be investigated using pathway analysis, knockdown experiments, and overexpression models.
CAB1 expression can be assessed using techniques such as qPCR, Western blotting, or immunohistochemistry.
The influence of genetic mutations on CAB1 function can be studied using in vitro assays and genetic databases.
Customer Reviews (3)
Write a reviewDependable results, a pillar of our research integrity.
Affordable protein assays, ideal for our budget allocation.
Professional expertise, accelerates our research endeavors.
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