Thermo Fisher Scientific ATP6V1F Polyclonal Antibody
Thermo Fisher Scientific의 ATP6V1F Polyclonal Antibody는 인간 V-ATPase F 서브유닛을 인식하는 토끼 IgG 폴리클로날 항체입니다. IHC(P)에서 1:500–1:1,000 희석으로 사용 가능하며, 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용됩니다.
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Applications
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:500–1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human V-ATPase F. Recombinant protein control fragment (Product #RP-103033) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.4 mg/mL |
| Purification | Antigen 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_2649406 |
Product Specific Information
- Immunogen sequence: DTFRSLGSLP GSVVEANPNQ RDPPLWDEID SRQFL
- Highest antigen sequence identity to orthologs:
- Mouse: 34%
- Rat: 37%
Target Information
ATP6V1F encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase–dependent organelle acidification is essential for intracellular processes such as:
- Protein sorting
- Zymogen activation
- Receptor-mediated endocytosis
- Synaptic vesicle proton gradient generation
V-ATPase is composed of:
- V1 domain (cytosolic): Three A and three B subunits, two G subunits, plus C, D, E, F, and H subunits — contains ATP catalytic site
- V0 domain (transmembrane): Five different subunits (a, c, c′, c″, and d)
Additional isoforms of V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. The encoded protein is the V1 domain F subunit protein.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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