
Thermo Fisher Scientific COL1A2 Polyclonal Antibody
COL1A2 단백질을 인식하는 Rabbit Polyclonal Antibody로, 인간 시료에 반응합니다. ICC/IF에 적합하며, 고순도의 Affinity chromatography로 정제되었습니다. PBS 기반 버퍼에 보관되며, 단기 4°C, 장기 -20°C 보관이 권장됩니다.
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Applications
Immunocytochemistry (ICC/IF)
- Tested Dilution: 0.25–2 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence (range: 1191–1265) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.2, with 40% glycerol |
| Contains | 0.02% 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_3092032 |
Product Specific Information
Immunogen sequence:
IKVYCDFSTG ETCIRAQPEN IPAKNWYRSS KDKKHVWLGE TINAGSQFEY NVEGVTSKEM ATQLAFMRLL ANYAS
Antigen sequence identity:
- Mouse: 83%
- Rat: 81%
Target Information
The COL1A2 gene encodes the pro-alpha2 chain of type I collagen, which forms a triple helix composed of two alpha1 chains and one alpha2 chain. Type I collagen is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis, and tendon.
Mutations in this gene are associated with:
- Osteogenesis imperfecta types I–IV
- Ehlers-Danlos syndrome type VIIB
- Recessive Ehlers-Danlos syndrome Classical type
- Idiopathic osteoporosis
- Atypical Marfan syndrome
Symptoms linked to COL1A2 mutations are generally less severe than those caused by COL1A1 mutations, reflecting the distinct structural role of alpha2 chains in matrix integrity. Three transcripts have been identified for this gene, resulting from alternate polyadenylation signals.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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