| Long name: |
Heparan Sulfate Proteoglycan 2 Antibody |
| Also known as: |
Heparan Sulfate Proteoglycan 2 Antibody |
| Category: |
Primary Antibodies |
| Conjugation: |
Unconjugated |
| Target Antigen: |
Heparan Sulfate Proteoglycan 2 |
| Specificity: |
This is a highly specific antibody against Heparan Sulfate Proteoglycan 2 |
| Modification(s): |
None |
| Modification site(s): |
Unmodified antibody |
| Clonality: |
Polyclonal antibody |
| Clone number: |
Polyclonal antibody |
| Concentration: |
1ug per 1ul |
| Source: |
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human Heparan Sulfate Proteoglycan 2 |
| Gene ID number: |
117194 |
| Tested Applications: |
IF(IHC-P), IHC-P |
| Recommended dilutions: |
IF(IHC-P)(1:50-200), IHC-P(1:100-500) |
| Cross reactivity: |
Mouse, Rat, Human |
| Cross reactive species details: |
not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Background of the target antigen: |
FBLN2, FGF2) activity and thus stimulate endothelial growth and re-generation, FGF7 and Transthyretin, FGFBP1, It can also promote growth factor (e, It has been shown that this protein interacts with laminin, It is a major component of basement membranes, It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis, Mar 2010], Mutations in this gene cause Schwartz-Jampel syndrome type 1, Perlecan is a key component of the vascular extracellular matrix, Silverman-Handmaker type of dyssegmental dysplasia, The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules, and Tardive dyskinesia, and plays essential roles in multiple biological activities, collagen type IV, etc, prolargin, where it helps to maintain the endothelial barrier function, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion, which consists of a core protein to which three long chains of glycosaminoglycans(heparan sulfate or chondroitin sulfate) are attached, This gene encodes the perlecan protein, [provided by RefSeq, g |
| Purification method: |
This antibody was purified via Protein A |
| Storage conditions: |
50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA |
| Synonym names: |
Basement membrane specic heparan sulfate proteoglycan core protein, Endorepellin domain V region, HSPG, HSPG 2, Heparan Sulfate Proteoglycan, Heparan sulfate proteoglycan of basement membrane, Hspg2, LG3 peptide, PLC antibody Schwartz Jampel syndrome 1 chondrodystrophic myotonia, Perlecan, SJA antibody SJS antibody SJS1 antibody, Perlecan |
| Properties: |
C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24° |
| Gene target: |
Heparan Sulfate Proteoglycan 2 |
| Short name: |
Heparan Sulfate Proteoglycan 2 Antibody |
| Technique: |
antibodies against human proteins, antibodies for, Antibody |
| Alternative name: |
Heparan Sulfate Proteoglycan 2 (Antibody to) |
| Alternative technique: |
antibodies |
| Identity: |
10893 |
| Gene: |
SJS1 |
More about : SJS1 |
| Long gene name: |
heparan sulfate proteoglycan 2 |
| Synonyms gene name: |
Schwartz-Jampel syndrome 1 (chondrodystrophic myotonia) |
| Synonyms: |
perlecan PRCAN HSPG2 |
| Synonyms name: |
perlecan proteoglycan |
| Locus: |
1p36, 12 |
| Discovery year: |
1991-02-27 |
| GenBank acession: |
M85289 |
| Entrez gene record: |
3339 |
| Pubmed identfication: |
1685141 11941538 |
| RefSeq identity: |
NM_005529 |
| Classification: |
I-set domain containing Proteoglycans Immunoglobulin like domain containing |
| Havana BLAST/BLAT: |
OTTHUMG00000002674 |