Clathrin (AA 4-171) 抗体

ABIN968006 产品详细信息, 供应商: Log in to see
抗原
  • CG9012
  • CHC
  • CLH
  • Cla
  • D-Chc
  • Dmel\\CG9012
  • chc
  • dCHC
  • l(1)13Fb
  • l(1)G0438
  • l(1)VI
  • CG6948
  • CLC
  • Dmel\\CG6948
  • clc
  • Clathrin heavy chain
  • Clathrin light chain
  • Chc
  • Clc
抗原表位
AA 4-171
2
1
1
1
1
1
1
适用
小鸡, 犬, 人, 小鼠, 大鼠
8
6
5
4
2
1
1
1
宿主
小鼠
11
2
克隆类型 (克隆位点)
单克隆 ()
应用范围
BioImaging (BI), Immunofluorescence (IF), Immunoprecipitation (IP), Immunohistochemistry (IHC), Western Blotting (WB)
12
9
7
6
3
2
1
1
1
1
选项
Supplier
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'独立验证'标志
Lot Number 14494
Method validated Immunohistochemistry
Positive Control Brain
Negative Control White adipose tissue
Notes Signal was detected in positive control sample and not in negative control sample.
Primary Antibody
  • Antibody: Clathrin (AA 4-171,Heavy Chain)
  • Catalog number: ABIN968006
  • Supplier: Log in to see
  • Supplier catalog number: Log in to see
  • Lot number: 14494
Isotype Control Antibody
Secondary Antibody
Controls
  • Positive control: rat cerebellum (specimen known to contain the target protein) from Explora BioLabs.
  • Negative Control: white adipose tissue (specimen known to not contain the target protein) from Explora
  • BioLabs.
  • Primary antibody isotype control: rat cerebellum treated with primary antibody isotype control instead of
  • the primary antibody.
  • Secondary antibody only control: rat cerebellum treated with secondary antibody only (no primary
  • antibody).
实验流程
  • Immunohistochemistry was performed on a Leica Bond automated immunostainer.
  • Sections were deparaffinized with Novocastra Bond Dewax Solution and rehydrated into Leica Bond
  • Wash Buffer.
  • Sections were heated to 98°C for 20 minutes in Tris buffer pH 9.0 (ER2; Leica) for antigen retrieval.
  • Sections were blocked in 3% normal goat serum plus 0.1 % Triton-X100 for 10 min at room
  • temperature.
  • Sections were washed x 3 in Leica Bond Wash Buffer.
  • Sections were incubated with primary antibody diluted 1:100 in Universal Antibody Dilution Buffer
  • (Electron Microscopy Sciences, 25885-05) for 60 min at room temperature.
  • Sections were washed x 3 in Leica Bond Wash Buffer.
  • Sections were incubated with secondary antibody diluted 1:100 in Universal Antibody Dilution Buffer
  • (Electron Microscopy Sciences, 25885-05) for 60 min at room temperature..
  • Sections were washed x 4 in Leica Bond Wash Buffer.
  • Sections were washed x 1 in Distilled Water. Sections were incubated with Peroxide Block (Leica) for 10 min to block endogenous peroxidase.
  • Sections were washed x 4 in Leica Bond Wash Buffer.
  • Sections were incubated with DAB chromogenic substrate (Leica) for 10 min at RT.
  • Sections were washed x 3 in Distilled Water.
  • Sections were counterstained with hematoxylin (Leica) for 2 min.
  • Sections were washed x 1 in Distilled Water.
  • Sections were washed x 1 in Leica Bond Wash Buffer.
  • Sections were washed x 1 in Distilled Water.
  • Sections were dehydrated, mounted and photographed under a light microscope.
Experimental Notes - Nothing to note.
Validation Images
Immunohistochemistry validation image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Figure 1: Cerebellum stained with anti-Clathrin (brown) and counterstained in blue.
Immunohistochemistry validation image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Figure 2: White adipose tissue stained with anti-Clathrin (brown) and counterstained ...
Immunohistochemistry validation image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Figure 3: Cerebellum stained with isotype control (brown) and counterstained in blue.
Immunohistochemistry validation image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Figure 1: Cerebellum stained with secondary antibody only (brown) and counterstained ...
免疫原 Rat Clathrin Heavy Chain aa. 4-171
克隆位点 23-Clathrin Heavy Chain
亚型 IgG1
交叉反应 人, 小鸡, 犬, 小鼠
产品特性 1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
2. Please refer to us for technical protocols.
3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
纯化方法 The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
背景 Clathrin is the major protein component in the coat formed around pits and vesicles involved in receptor-mediated endocytosis. Clathrin forms a non-covalently bound triskelion structure composed of three heavy chains (192 kDa each) and three light chains (23-25 kDa each). Each leg of the triskelion structure contains one heavy and one light chain. The three heavy chains forming the triskelion structure are attached at their respective proximal ends like spokes on a wheel. Clathrin heavy chain is composed of a terminal globular domain, a distal segment containing several areas sensitive to enzymatic cleavage, and a proximal segment which contains a light chain binding site. The proximal and distal domains are connected by a joint segment at which there is a sharp bend in the heavy chains of fully-assembled triskelia. Although the calculated molecular weight is 192 kDa, clathrin heavy chain migrates at approximately 180 kDa.
分子量 180 kDa
研究领域 Transporters, Organelles
应用备注 Immunofluorescent Staining and Bioimaging Methanol Procedure for a 96 well plate: Remove media from wells. Add 100 µl/well fresh 3.7% Formaldehyde in PBS. Incubate for 10 minutes at room temperature (RT). Flick out and add 100 µl/well 90% methanol. Incubate for 5 minutes at RT. Flick out and wash twice with PBS. Flick out PBS and add 100 µl/well blocking buffer (3% FBS in PBS). Incubate for 30 minutes at RT. Flick out and add diluted antibody (diluted in blocking buffer). Incubate for 1 hour at RT. Wash three times with PBS. Flick out PBS and add second step reagent. Incubate for 1 hour at RT. Wash three times with PBS.
Triton-X 100 Procedure for a 96 well plate: Remove media from wells. Add 100 µl/well fresh 3.7% Formaldehyde in PBS. Incubate for 10 minutes at room temperature (RT). Flick out and add 100 µl/well 0.1% Triton-X 100. Incubate for 5 minutes at RT. Flick out and wash twice with PBS. Flick out PBS and add 100 µl/well blocking buffer (3% FBS in PBS). Incubate for 30 minutes at RT. Flick out and add diluted antibody (diluted in blocking buffer). Incubate for 1 hour at RT. Flick out and wash three times with PBS. Flick out and add second step reagent. Incubate for 1 hour at RT. Flick out and wash three times with PBS.
说明

Related Products: ABIN968535

限制 仅限研究用
状态 Liquid
浓度 0.25 mg/ml
缓冲液 Aqueous buffered solution containing BSA, glycerol, and ≤0.09 % sodium azide.
储存液 Sodium azide
注意事项 This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件 -20 °C
储存方法 Store undiluted at -20° C.
厂商提供的图像
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)) image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Rat cerebellum, zinc-fixed paraffin embedded tissue (left), 40X
Western Blotting (WB) image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Western blot analysis of Clathrin Heavy Chain on HeLa cell lysate (center). Lane 1: 1...
Immunofluorescence (IF) image for anti-Clathrin (AA 4-171) antibody (ABIN968006) Immunofluorescent staining of C6 cells (right). Cells were seeded in a collagen coate...
有引用在: Padilla, Chang, Pacheco-Rodriguez, Adamik, Moss, Vaughan: "Interaction of FK506-binding protein 13 with brefeldin A-inhibited guanine nucleotide-exchange protein 1 (BIG1): effects of FK506." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 100, Issue 5, pp. 2322-7, 2003 (PubMed).

Kalthoff, Groos, Kohl, Mahrhold, Ungewickell: "Clint: a novel clathrin-binding ENTH-domain protein at the Golgi." in: Molecular biology of the cell, Vol. 13, Issue 11, pp. 4060-73, 2002 (PubMed).

van Kerkhof, Sachse, Klumperman, Strous: "Growth hormone receptor ubiquitination coincides with recruitment to clathrin-coated membrane domains." in: The Journal of biological chemistry, Vol. 276, Issue 6, pp. 3778-84, 2001 (PubMed).

Okamoto, Karam, Jeng, Forte, Goldenring: "Identification of clathrin and clathrin adaptors on tubulovesicles of gastric acid secretory (oxyntic) cells." in: The American journal of physiology, Vol. 274, Issue 4 Pt 1, pp. C1017-29, 1998 (PubMed).

Liu, Wong, Craik, Brodsky: "Regulation of clathrin assembly and trimerization defined using recombinant triskelion hubs." in: Cell, Vol. 83, Issue 2, pp. 257-67, 1995 (PubMed).

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