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Collagen Type XXVIII Polyclonal antibody, PBS Only

Collagen Type XXVIII Polyclonal Antibody for WB, IF/ICC, Indirect ELISA

Cat No. 24401-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, IF/ICC, Indirect ELISA

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

24401-1-PBS targets Collagen Type XXVIII in WB, IF/ICC, Indirect ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag21459

Product name: Recombinant human COL28A1 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 34-295 aa of BC136892

Sequence: LARKSDVQGSICFIDIVFIVDSSESSKIALFDKQKDFVDSLSDKIFQLTPGRSLEYDIKLAALQFSSSVQIDPPFSSWKDLQTFKQKVKSMNLIGQGTFSYYAISNATRLLKREGRKDGVKVVLLMTDGIDHPKNPDVQSISEDARISGISFITIGLSTVVNEAKLRLISGDSSSEPTLLLSDPTLVDKIQDRLDILFEKKCERKICECEKGDPGDPGPPGTHGNPGIKGERGPKGNPGNAQKGEAGERGPGGIPGYKGDKG

Predict reactive species
Full Name collagen, type XXVIII, alpha 1
Calculated Molecular Weight 1125 aa, 117 kDa
Observed Molecular Weight72 kDa, 100-117 kDa
GenBank Accession NumberBC136892
Gene Symbol COL28A1
Gene ID (NCBI) 340267
RRIDAB_3669435
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ2UY09
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

COL28A1 (collagen type XXVIII alpha 1 chain), also known as COL28. It is expected to be located in the basement membranes, cytoplasm and nucleus. And the protein is mainly expressed in salivary gland and adrenal. This antibody can recognize the 117 kDa and 72 kDa isoforms of target. COL28A1 is a new collagen that cannot clearly be assigned to any collagen subgroup, despite the fact that it contains VWA domains. Ongoing investigations will shed further light on the role of COL28A1 in the assembly of nerve fiber basement membranes. Although no human mutation has been associated with COL28A1, it is tempting to speculate that mutations in this gene would lead to neurodegenerative disease (PMID: 16330543).

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