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Thermo Fisher Scientific Collagen II Monoclonal Antibody (2B1.5)
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Thermo Fisher Scientific Collagen II Monoclonal Antibody (2B1.5)

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Type II collagen에 특이적인 mouse monoclonal antibody로, cartilage 연구 및 질병 관련 단백질 분석에 적합함. Western blot, IHC, ICC 등 다양한 응용 가능. Protein A로 정제된 액상 제품으로 안정적인 성능 제공.

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pk
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마지막 업데이트 2025. 08. 04. 오후 06:15
Thermo Fisher Scientific MA137493 Collagen II Monoclonal Antibody (2B1.5) 200 ug pk판매 단위 pk ·
재고 확인 필요
1,160,300원VAT 포함 1,276,330원
Thermo Fisher Scientific MA512789 Collagen II Monoclonal Antibody (2B1.5) 500 ul pk판매 단위 pk
재고 1개
759,000원VAT 포함 834,900원

Thermo Fisher Scientific · Thermo Fisher Scientific Collagen II Monoclonal Antibody (2B1.5)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:50 View 10 publications
Immunohistochemistry (IHC) - View 60 publications
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:400 View 2 publications
Immunohistochemistry (Frozen) (IHC (F)) - View 1 publication
Immunocytochemistry (ICC/IF) - View 15 publications
Flow Cytometry (Flow) Assay-dependent View 2 publications
Miscellaneous PubMed (Misc) - View 1 publication

Product Specifications

Item Description
Species Reactivity Bovine, Chicken, Human, Mouse, Rat
Published Species Bovine, Goat, Guinea pig, Human, Mouse, Pig, Rabbit, Rat, Sheep
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 2B1.5
Immunogen Purified preparation of lathyritic type II collagen from embryonic chicken sternum
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.4, with 0.2% BSA
Contains 0.09% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2082337

Additional Formats:


Product Specific Information

Staining of formalin/paraffin tissues requires digestion of tissue sections with pepsin at 1 mg/mL Tris-HCl, pH 2.0 for 15 min at room temperature or 10 min at 37°C.


Target Information

COL2A1 encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye.
Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type.
Defects in processing chondrocalcin, a calcium-binding protein that is the C-propeptide of this collagen molecule, are also linked to chondrodysplasia.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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