pAb; Rabbit anti Human TGFBI Antibody; WB, IHC; Unconjugated
| SKU | Size | Availability | Price | Qty |
|---|---|---|---|---|
| Ab130905-10μl | 10μl | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $59.90 | |
| Ab130905-20μl | 20μl | In stock | $89.90 | |
| Ab130905-50μl | 50μl | In stock | $179.90 | |
| Ab130905-100μl | 100μl | In stock | $279.90 | |
| Ab130905-1ml | 1ml | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $2,399.90 |
pAb; Rabbit anti Human TGFBI Antibody; WB, IHC; Unconjugated
| Product Name | TGFBI Antibody - Primary antibody, specific to TGFBI, Rabbit IgG |
|---|---|
| Synonyms | RGD containing collagen associated protein antibody; AI181842 antibody; AI747162 antibody; Beta ig antibody; Beta ig h3 antibody; Beta ig-h3 antibody; BGH3_HUMAN antibody; Big h3 antibody; BIGH3 antibody; CDB1 antibody; CDG2 antibody; CDGG1 antibody; CSD |
| Specifications & Purity | ExactAb™, Validated, Carrier Free, High performance, Lot by Lot |
| Host species | Rabbit |
| Specificity | TGFBI |
| Immunogen | Recombinant TGFBI expressed in E.coli (AA 423-632). |
| Positive Control | WB: HeLa and A549 cell lysates. IHC: Human stomach, glioma, liver and kidney tissues. |
| Conjugation | Unconjugated |
| Grade | Carrier Free, ExactAb™, High Performance, Validated |
| Product Description | Rabbit anti Human TGFBI Antibody, Polyclonal, could be used for WB, IHC and so on. |
| Isotype | Rabbit IgG |
|---|---|
| SDS-PAGE | 150 kDa |
| Purification Method | Antigen affinity purified + Protein A purified |
| Form | Liquid |
| Concentration | Lot by Lot |
| Storage Temp | Store at -20°C,Avoid repeated freezing and thawing |
| Shipped In | Ice chest + Ice pads |
| Stability And Storage | Store at 4℃ short term (1-2 weeks). Store at -20℃ long term (24 months). Upon delivery aliquot. Avoid freeze/thaw cycle. |
TGFBI Antibody (Ab130905) - Western Blot
All lanes: TGFBI Antibody (Ab130905) at 1/1000 dilution
Samples: Lysates at 20 µg per lane
Secondary: Goat Anti-Rabbit IgG H&L (HRP) (Ab170144) at 1/20000 dilution
Predicted band size: 75 kDa
Observed band size: 72 kDa
Exposure time: 40.7 s
TGFBI Antibody (Ab130905) - IHC
DAB staining on IHC
Samples: Human Stomach Tissue
Primary Ab: 20 µg/mL TGFBI Antibody (Ab130905)
Second Ab: 2 µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody
TGFBI Antibody (Ab130905) - IHC
DAB staining on IHC
Samples: Human Glioma Tissue
Primary Ab: 20 µg/mL TGFBI Antibody (Ab130905)
Second Ab: 2 µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody
TGFBI Antibody (Ab130905) - IHC
DAB staining on IHC
Samples: Human Liver Tissue
Primary Ab: 20 µg/mL TGFBI Antibody (Ab130905)
Second Ab: 2 µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody
TGFBI Antibody (Ab130905) - IHC
DAB staining on IHC
Sample: Human Kidney Tissue
Primary Ab: 20 μg/mL TGFBI Antibody (Ab130905)
Second Ab: 2 µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Application | Dilution info |
|---|---|
| IHC | 5-20 µg/mL |
| WB |
0.01-2 µg/mL
|
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 ZJ23F1202106 | Certificate of Analysis | Dec 20, 2023 | Ab130905 |
| ZJ23F1202105 | Certificate of Analysis | Dec 20, 2023 | Ab130905 |
| ZJ23F1202104 | Certificate of Analysis | Dec 20, 2023 | Ab130905 |
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| 6. Korvatska, E E and 13 more authors.. (1998) Mutation hot spots in 5q31-linked corneal dystrophies.. American journal of human genetics, [PMID:9463327] |
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| 8. Okada, M M and 10 more authors.. (1998) Two distinct kerato-epithelin mutations in Reis-Bücklers corneal dystrophy.. American journal of ophthalmology, [PMID:9780098] |
| 9. Fujiki, K K and 6 more authors.. (1998) A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities.. Human genetics, [PMID:9799082] |
| 10. Stewart, H H and 7 more authors.. (1999) A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.. Ophthalmology, [PMID:10328397] |
| 11. Stewart, H S HS and 5 more authors.. (1999) Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis.. Human mutation, [PMID:10425035] |
| 12. Rozzo, C C and 7 more authors.. (1998) A common beta ig-h3 gene mutation (delta f540) in a large cohort of Sardinian Reis Bücklers corneal dystrophy patients. Mutations in brief no. 180. Online.. Human mutation, [PMID:10660331] |
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| 14. Dighiero, P P and 5 more authors.. (2000) A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126.. Archives of ophthalmology (Chicago, Ill. : 1960), [PMID:10865320] |
| 15. Mashima, Y Y and 8 more authors.. (2000) Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan.. American journal of ophthalmology, [PMID:11024425] |
| 16. Dighiero, P P and 7 more authors.. (2001) Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene.. Ophthalmology, [PMID:11297504] |
| 17. Hirano, K K and 5 more authors.. (2001) Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.. Cornea, [PMID:11413411] |
| 18. Fujiki, K K, Nakayasu, K K and Kanai, A A.. (2001) Corneal dystrophies in Japan.. Journal of human genetics, [PMID:11501939] |
| 19. Munier, Francis L FL and 19 more authors.. (2002) BIGH3 mutation spectrum in corneal dystrophies.. Investigative ophthalmology & visual science, [PMID:11923233] |
| 20. Ha, Nguyen Thanh NT and 6 more authors.. () A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy.. Japanese journal of ophthalmology, [PMID:12782158] |
| 21. Warren, John F JF and 5 more authors.. (2003) A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.. American journal of ophthalmology, [PMID:14597039] |
| 22. Schmutz, Jeremy J and 75 more authors.. (2004) The DNA sequence and comparative analysis of human chromosome 5.. Nature, (16): [PMID:15372022] |
| 23. Aldave, Anthony J AJ and 8 more authors.. (2004) Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.. American journal of ophthalmology, [PMID:15531312] |
| 24. Chakravarthi, S V V Kalyana SV, Kannabiran, Chitra C, Sridhar, Mittanamalli S MS and Vemuganti, Geeta K GK.. (2005) TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.. Investigative ophthalmology & visual science, [PMID:15623763] |
| 25. Stix, Barbara B and 10 more authors.. (2005) Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.. Investigative ophthalmology & visual science, [PMID:15790870] |
| 26. Tian, Xin X and 6 more authors.. () Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I.. Japanese journal of ophthalmology, [PMID:15838722] |
| 27. Aldave, Anthony J AJ, Rayner, Sylvia A SA, Kim, Brian T BT, Prechanond, Apiradi A and Yellore, Vivek S VS.. (2006) Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.. Molecular vision, (27): [PMID:16541014] |
| 28. Zenteno, Juan Carlos JC, Ramirez-Miranda, Arturo A, Santacruz-Valdes, Concepcion C and Suarez-Sanchez, Raul R.. (2006) Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy.. Molecular vision, (10): [PMID:16636649] |
| 29. Boutboul, Sandrine S and 8 more authors.. (2006) A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.. Human mutation, [PMID:16652336] |
| 30. Atchaneeyasakul, La-Ongsri LO and 6 more authors.. () A novel H572R mutation in the transforming growth factor-beta-induced gene in a Thai family with lattice corneal dystrophy type I.. Japanese journal of ophthalmology, [PMID:17013691] |
| 31. Coutu, Daniel L DL and 5 more authors.. (2008) Periostin, a member of a novel family of vitamin K-dependent proteins, is expressed by mesenchymal stromal cells.. The Journal of biological chemistry, (27): [PMID:18450759] |
| 32. Annis, Douglas S DS and 7 more authors.. (2015) Absence of Vitamin K-Dependent γ-Carboxylation in Human Periostin Extracted from Fibrotic Lung or Secreted from a Cell Line Engineered to Optimize γ-Carboxylation.. PloS one, [PMID:26273833] |
| 33. Lukassen, Marie V MV, Scavenius, Carsten C, Thøgersen, Ida B IB and Enghild, Jan J JJ.. (2016) Disulfide Bond Pattern of Transforming Growth Factor β-Induced Protein.. Biochemistry, (4): [PMID:27609313] |
