Rabbit Polyclonal Anti-COL12A1 antibody (STJ98958)


Reactivity: Human
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Rabbit Polyclonal Anti-COL12A1 antibody (STJ98958)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, ELISA

Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody


|BA209D8.1 antibody|COCA1 antibody|COL12A1 antibody|COL12A1L antibody|Collagen alpha-1(XII) chain antibody|collagen type XII proteoglycan antibody|collagen, type XII, alpha 1 antibody|DJ234P15.1 antibody|Anti-COL12A1 antibody (ab196619)
SCBT cat No: sc-166020|sc-68449|sc-68862|


Anti-COL12A1 antibody

Catalogue No.





Anti-COL12A1 antibody detects endogenous COL12A1.


Synthetic peptide from human protein at AA range: 1993-2064.





Recommended dilution

WB 1:500-2000; ELISA 1:10000-20000








Anti-COL12A1 antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.


1 mg/ml


Anti-COL12A1 antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.


-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

BA209D8.1 antibody, COCA1 antibody, COL12A1 antibody, COL12A1L antibody, Collagen alpha-1(XII) chain antibody, collagen type XII proteoglycan antibody, collagen, type XII, alpha 1 antibody, DJ234P15.1 antibody

Database links


Protein function

Type XII collagen interacts with type I collagen-containing fibrils, the COL1 domain could be associated with the surface of the fibrils, and the COL2 and NC3 domains may be localized in the perifibrillar matrix. .

Protein tissue specificity

Found in collagen I-containing tissues: both isoform 1 and isoform 2 appear in amnion, chorion, skeletal muscle, small intestine, and in cell culture of dermal fibroblasts, keratinocytes and endothelial cells. Only isoform 2 is found in lung, placenta, kidney and a squamous cell carcinoma cell line. Isoform 1 is also present in the corneal epithelial Bowman’s membrane (BM) and the interfibrillar matrix of the corneal stroma, but it is not detected in the limbal BM. .

Involvement in disease

Ullrich congenital muscular dystrophy 2 (UCMD2) [MIM:616470]: A form of Ullrich muscular dystrophy, a congenital myopathy characterized by muscle weakness and multiple joint contractures, generally noted at birth or early infancy. The clinical course is more severe than in Bethlem myopathy. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Bethlem myopathy 2 (BTHLM2) [MIM:616471]: A form of Bethlem myopathy, a benign proximal myopathy characterized by early childhood onset and joint contractures most frequently affecting the elbows and ankles. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the fibril-associated collagens with interrupted helices (FACIT) family. ; Contains 4 collagen-like domains. ; Contains 18 fibronectin type-III domains. ; Contains 1 laminin G-like domain. ; Contains 4 VWFA domains.

Protein post-translational modifications

The triple-helical tail is stabilized by disulfide bonds at each end. .; Hydroxylation on proline residues within the sequence motif, GXPG, is most likely to be 4-hydroxy as this fits the requirement for 4-hydroxylation in vertebrates. .; Isoform 1 O-glycosylation; glycosaminoglycan of chondroitin-sulfate type. .

Protein cellular localization

Secreted, extracellular space, extracellular matrix .


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St John’s Laboratory Ltd.

Product type

Primary antibody


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