Recombinant Human TGFBI, His tagged
Cat.No. : | TGFBI-210H |
Product Overview : | Recombinant Human TGFBI precursor extracellular domain (NP_000349.1) (Met 1-His 683), fused with a polyhistidine tag at the C-terminus, was produced in Human Cell. |
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Source : | HEK293 |
Species : | Human |
Tag : | His |
Form : | Lyophilized from sterile PBS, pH 7.4 |
Molecular Mass : | The secreted recombinant human beta IG-H3 comprises 671 amino acids with a predicted molecular mass of 74 kDa. As a result of glycosylation, the apparent molecular mass of rh beta IG-H3 is approximately 65 kDa in SDS-PAGE under reducing conditions. |
Protein Length : | Met 1-His 683 |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method |
Purity : | > 75 % as determined by SDS-PAGE |
Storage : | Samples are stable for up to twelve months from date of receipt at -20°C to -80°C Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
Reconstitution : | It is recommended that sterile water be added to the vial to prepare a stock solution of 0.2 ug/ul. Centrifuge the vial at 4°C before opening to recover the entire contents. |
Gene Name : | TGFBI transforming growth factor, beta-induced, 68kDa [ Homo sapiens ] |
Official Symbol : | TGFBI |
Synonyms : | TGFBI; transforming growth factor, beta-induced, 68kDa; CSD1, CSD2, CSD3, LCD1, transforming growth factor, beta induced, 68kD; transforming growth factor-beta-induced protein ig-h3; BIGH3; CDB1; CDGG1; RGD-CAP; beta ig-h3; kerato-epithelin; RGD-containing collagen-associated protein; CSD; CDG2; CSD1; CSD2; CSD3; EBMD; LCD1; |
Gene ID : | 7045 |
mRNA Refseq : | NM_000358 |
Protein Refseq : | NP_000349 |
MIM : | 601692 |
UniProt ID : | Q15582 |
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◆ Lysates | ||
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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 (5)
Ask a questionTGFBI protein is essential for maintaining the structure and transparency of the cornea, a clear, dome-shaped outermost layer of the eye.
Mutations or abnormalities in the TGFBI protein can lead to various corneal dystrophies, which are inherited eye disorders that affect vision.
In severe cases, these dystrophies can lead to vision impairment or blindness. Early diagnosis, appropriate treatment, and regular eye care can help prevent or delay vision loss.
TGFBI mutations are typically diagnosed through genetic testing, corneal examinations, and medical history.
Customer Reviews (3)
Write a reviewHighly recommended and known for its outstanding performance in ELISA, the TGFBI protein is a top choice for researchers in protein electron microscopy structure analysis.
By utilizing the TGFBI protein, researchers can confidently explore the intricate details of protein structures and gain invaluable insights into their functionality.
Its exceptional properties and reliable results make it a valuable tool in various experimental applications.
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