Anti-COL10A1 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-COL10A1 Antibody (CSB-PA005715ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

COL10A1 Antibody

More alternative names for the antibody
COAA1_HUMAN antibody|Col10a 1 antibody|COL10A1 antibody|Collagen alpha 1(X) chain antibody|Collagen alpha-1(X) chain antibody|Collagen type X alpha 1 (Schmid metaphyseal chondrodysplasia) antibody|Collagen type X alpha 1 antibody|Collagen X alpha 1 polypeptide antibody|CollagenX antibody|fa66d11 antibody|fb10c08 antibody|OTTHUMP00000040411 antibody|Procollagen type X alpha 1 antibody|Schmid metaphyseal chondrodysplasia antibody|wu:fa66d11 antibody|wu:fb10c08 antibody
Anti-Collagen X antibody (ab58632)
Close sc-323750|sc-323751|

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-COL10A1 Antibody

Catalogue No.

CSB-PA005715ESR2HU

Reactivity

Human

Immunogen

Recombinant human Collagen alpha-1(X) chain protein (521-680AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

66 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:282416( Cow), Entrez Gene:1300( Human), Entrez Gene:12813( Mouse), Entrez Gene:25681( Rat), Omim:120110( Human), SwissProt:P23206( Cow), SwissProt:Q03692( Human), SwissProt:Q05306( Mouse), Unigene:520339( Human), Unigene:443177( Mouse), Unigene:20579( Rat)

Protein function

Type X collagen is a product of hypertrophic chondrocytes and has been localized to presumptive mineralization zones of hyaline cartilage.

Involvement in disease

Schmid type metaphyseal chondrodysplasia (SMCD) [MIM:156500]: Dominantly inherited disorder of the osseous skeleton. The cardinal features of the phenotype are mild short stature, coxa vara and a waddling gait. Radiography usually shows sclerosis of the ribs, flaring of the metaphyses, and a wide irregular growth plate, especially of the knees. A variant form of SMCD is spondylometaphyseal dysplasia Japanese type. It is characterized by spinal involvement comprising mild platyspondyly, vertebral body abnormalities, and end-plate irregularity. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein post-translational modifications

Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.

Protein cellular localization

Secreted, extracellular space, extracellular matrix .

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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