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Thermo Fisher Scientific Collagen III Monoclonal Antibody (FH-7A)
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Thermo Fisher Scientific Collagen III Monoclonal Antibody (FH-7A)

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Collagen III에 특이적인 FH-7A 클론 단일클론 항체로 인간, 토끼, 랫트 시료에 반응. WB, IHC, ELISA 등 다양한 응용 가능. 비결합형 액상 형태로 4 mg/mL 농도. 단기 4°C, 장기 -20°C 보관 권장.

카탈로그번호
MA122147
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 05:58
Thermo Fisher Scientific MA122147 Collagen III Monoclonal Antibody (FH-7A) 100 ul pk판매 단위 pk ·
재고 확인 필요
827,000원VAT 포함 909,700원

Thermo Fisher Scientific · Thermo Fisher Scientific Collagen III Monoclonal Antibody (FH-7A)

Applications

Application Tested Dilution Publications
Western Blot (WB) Assay-dependent View 3 publications
Immunohistochemistry (IHC) - View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent -
Immunohistochemistry (Frozen) (IHC (F)) 1:4,000 -
ELISA Assay-dependent -
Dot blot (DB) Assay-dependent -

Product Specifications

Specification Description
Species Reactivity Human, Rabbit, Rat
Published Species Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone FH-7A
Immunogen Human collagen type III protein
Conjugate Unconjugated
Form Liquid
Concentration 4 mg/mL
Storage Buffer Ascites
Contains 15 mM sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_558480

Product Specific Information

  • Recommended positive controls: human skin
  • MA1-22147 specifically recognizes native and denatured collagen type III in human and rat samples.
  • Does not recognize collagen types I, II, IV, V, VI, and X.
  • In Western blot, detects a ~70 kDa band in reduced denatured samples and a ~300 kDa band in non-reduced, non-denatured samples.
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Collagen III is a fibrillar collagen found in extensible connective tissues such as skin, lung, and the vascular system, often associated with type I collagen.
Mutations in the gene are linked to Ehlers-Danlos syndrome type IV and aortic or arterial aneurysms.
Alternate transcripts detected for this gene are mutation-derived and cause exon exclusion due to altered splicing.


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

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