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Thermo Fisher Scientific COL11A2 Polyclonal Antibody
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Thermo Fisher Scientific COL11A2 Polyclonal Antibody

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Rabbit polyclonal antibody against human COL11A2 for Western blot applications. Recognizes N-terminal region recombinant protein. High specificity and affinity-purified. Suitable for research use only.

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마지막 업데이트 2025. 08. 05. 오후 03:13
Thermo Fisher Scientific PA585501 COL11A2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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657,900원VAT 포함 723,690원

Thermo Fisher Scientific · Thermo Fisher Scientific COL11A2 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:1,000–1:10,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein encompassing a sequence within the N-terminus region of human COL11A2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol
Contains 0.01% thimerosal
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_2792641

Product Specific Information

  • Keep as concentrated solution.
  • Predicted reactivity: Mouse (85%), Rat (85%), Bovine (93%).
  • Positive Control: human COL11A2-transfected 293T cells (partial fragment).
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain.
Mutations in this gene are associated with:

  • Type III Stickler syndrome
  • Otospondylomegaepiphyseal dysplasia (OSMED syndrome)
  • Weissenbacher-Zweymuller syndrome
  • Autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13)
  • Autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53)

Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6.


WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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