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MATN1 产品

(Matrilin 1, Cartilage Matrix Protein (MATN1))
This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. Mutations of this gene have been associated with variety of inherited chondrodysplasias. [provided by RefSeq, Jul 2008].

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Featured MATN1 Categories

MATN1 抗体

High quality antibodies with extensive validation data.

MATN1 ELISA试剂盒

Reliable ELISA kits for a wide range of species.

MATN1 蛋白

Proteins for various applications incl. WB, ELISA, IF etc.

Recommended MATN1 抗体

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Application ELISA, ICC
Validations
  • (1)
  • (2)
Cat. No. ABIN969278
Quantity 100 μL
Datasheet Datasheet
Reactivity Mouse
Application WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro)
Validations
  • (1)
  • (1)
Cat. No. ABIN676178
Quantity 100 μL
Datasheet Datasheet
Reactivity Human, Mouse, Rat
Application WB, ELISA, IHC, IHC (p)
Validations
  • (2)
Cat. No. ABIN605084
Quantity 0.05 mg
Datasheet Datasheet

Recommended MATN1 ELISA试剂盒

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Rat
Analytical Method Quantitative Competition ELISA
Validations
Cat. No. ABIN510637
Quantity 96 tests
Datasheet Datasheet

Recommended MATN1 蛋白

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Chicken
Source Yeast
Validations
Cat. No. ABIN1459156
Quantity 1 mg
Datasheet Datasheet

Latest Publications for our MATN1 Products

Park, Woo, Lee: "Ionically cross-linkable hyaluronate-based hydrogels for injectable cell delivery." in: Journal of controlled release : official journal of the Controlled Release Society, (2014) (PubMed).

Bell, Piróg, Fresquet, Thornton, Boot-Handford, Briggs: "Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation." in: Arthritis and rheumatism, Vol. 64, Issue 5, pp. 1529-39, (2012) (PubMed).

Chamberlin, Ubagai, Mudd, Thomas, Pao, Nguyen, Levy, Greene, Freehauf, Chou: "Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations." in: American journal of human genetics, Vol. 66, Issue 2, pp. 347-55, (2000) (PubMed).

Synonyms and alternative names related to MATN1

matrilin 1, cartilage matrix protein L homeolog (matn1.L), matrilin 1 (matn1), matrilin 1, cartilage matrix protein (MATN1), matrilin 1, cartilage matrix protein (matn1), matrilin 1, cartilage matrix protein (Matn1), cmp, CMP, crtm, CRTM, Crtm, Mat1, matrilin-1, MGC64509, MGC108367, xmatn1

Protein level used designations for MATN1

  • matrilin 1, cartilage matrix protein
  • matrilin 1
  • cartilage matrix protein
  • cartilage matrix protein-like
  • matrilin 1, cartilage matrix protein 1
  • matrilin-1
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