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Mouse Anti-COL9A1 Recombinant Antibody (CBCNC-053) (CBMAB-C0946-CN)

This product is a Mouse antibody that recognizes COL9A1. The antibody CBCNC-053 can be used for immunoassay techniques such as: WB.
See all COL9A1 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBCNC-053
Antibody Isotype
IgG2a, κ
Application
WB

Basic Information

Specificity
Human
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Buffer
PBS, pH 7.2
Preservative
No preservatives

Target

Full Name
Collagen Type IX Alpha 1 Chain
Introduction
COL9A1 (Collagen Type IX Alpha 1 Chain) is a Protein Coding gene. Diseases associated with COL9A1 include Epiphyseal Dysplasia, Multiple, 6 and Stickler Syndrome, Type Iv. Among its related pathways are Integrin Pathway and ERK Signaling. Gene Ontology (GO) annotations related to this gene include extracellular matrix structural constituent conferring tensile strength. An important paralog of this gene is COL9A2.
Entrez Gene ID
1297
UniProt ID
P20849
Alternative Names
Collagen Type IX Alpha 1 Chain; Collagen, Type IX, Alpha 1; Cartilage-Specific Short Collagen; Collagen IX, Alpha-1 Polypeptide; Alpha-1(IX) Collagen Chain; Collagen Alpha-1(IX) Chain;
Function
Structural component of hyaline cartilage and vitreous of the eye.
Biological Process
Animal organ morphogenesis Source: ProtInc
Collagen fibril organization Source: Reactome
Extracellular matrix organization Source: GO_Central
Cellular Location
Extracellular matrix
Involvement in disease
Multiple epiphyseal dysplasia 6 (EDM6):
A generalized skeletal dysplasia associated with significant morbidity. Joint pain, joint deformity, waddling gait, and short stature are the main clinical signs and symptoms. Radiological examination of the skeleton shows delayed, irregular mineralization of the epiphyseal ossification centers and of the centers of the carpal and tarsal bones. Multiple epiphyseal dysplasia is broadly categorized into the more severe Fairbank and the milder Ribbing types. The Fairbank type is characterized by shortness of stature, short and stubby fingers, small epiphyses in several joints, including the knee, ankle, hand, and hip. The Ribbing type is confined predominantly to the hip joints and is characterized by hands that are normal and stature that is normal or near-normal.
Stickler syndrome 4 (STL4):
An autosomal recessive form of Stickler syndrome, an inherited disorder that associates ocular signs with more or less complete forms of Pierre Robin sequence, bone disorders and sensorineural deafness. Ocular disorders may include juvenile cataract, myopia, strabismus, vitreoretinal or chorioretinal degeneration, retinal detachment, and chronic uveitis. Pierre Robin sequence includes an opening in the roof of the mouth (a cleft palate), a large tongue (macroglossia), and a small lower jaw (micrognathia). Bones are affected by slight platyspondylisis and large, often defective epiphyses. Juvenile joint laxity is followed by early signs of arthrosis. The degree of hearing loss varies among affected individuals and may become more severe over time. Syndrome expressivity is variable.
PTM
Covalently linked to the telopeptides of type II collagen by lysine-derived cross-links.
Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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