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TGFBI Antibody - Primary antibody, specific to TGFBI, Rabbit IgG

  • Carrier Free
  • ExactAb™
  • High performance
  • Validated
  • Lot by Lot
Features and benefits
  • Short Overview:

    pAb; Rabbit anti Human TGFBI Antibody; WB, IHC; Unconjugated

  • Species reactivity(Reacts with): Human,Mouse,Rat
  • Isotype: Rabbit IgG
    Application:
  • IHC
  • WB
Item Number
Ab130905
Grouped product items
SKUSizeAvailabilityPrice 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

View related series
Accession#:Q15582 Gene ID:7045 TGFBI

Basic Description

Product NameTGFBI Antibody - Primary antibody, specific to TGFBI, Rabbit IgG
SynonymsRGD 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 & PurityExactAb™, Validated, Carrier Free, High performance, Lot by Lot
Host speciesRabbit
SpecificityTGFBI
ImmunogenRecombinant TGFBI expressed in E.coli (AA 423-632).
Positive ControlWB: HeLa and A549 cell lysates. IHC: Human stomach, glioma, liver and kidney tissues.
ConjugationUnconjugated
GradeCarrier Free, ExactAb™, High performance, Validated
Product Description

Rabbit anti Human TGFBI Antibody, Polyclonal, could be used for WB, IHC and so on.
Application
WB: 0.01-2 μg/mL
IHC: 5-20 μg/mL
Protein Function
Binds to type I, II, and IV collagens. This adhesion protein may play an important role in cell-collagen interactions. In cartilage, may be involved in endochondral bone formation.

Product Properties

IsotypeRabbit IgG
SDS-PAGE150 kDa
Purification MethodAntigen affinity purified + Protein A purified
FormLiquid
ConcentrationLot by Lot
Storage TempStore at -20°C,Avoid repeated freezing and thawing
Shipped InIce chest + Ice pads
Stability And StorageStore at 4℃ short term (1-2 weeks). Store at -20℃ long term (24 months). Upon delivery aliquot. Avoid freeze/thaw cycle.

Images

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

Associated Targets

TGFBI Tbio Transforming growth factor-beta-induced protein ig-h3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Application

ApplicationDilution info
IHC

5-20 µg/mL

WB

0.01-2 µg/mL

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

3 results found

Lot NumberCertificate TypeDateItem
ZJ23F1202106Certificate of AnalysisDec 20, 2023 Ab130905
ZJ23F1202105Certificate of AnalysisDec 20, 2023 Ab130905
ZJ23F1202104Certificate of AnalysisDec 20, 2023 Ab130905

Related Documents

References

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7. Yamamoto, S S and 11 more authors..  (1998)  A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA..  American journal of human genetics,      [PMID:9497262]
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]
13. Hirano, K K, Hotta, Y Y, Fujiki, K K and Kanai, A A..  (2000)  Corneal amyloidosis caused by Leu518Pro mutation of betaig-h3 gene..  The British journal of ophthalmology,      [PMID:10837380]
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]

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