产品: DYNLL2 抗体
货号: DF12966
描述: Rabbit polyclonal antibody to DYNLL2
应用: WB
文献验证: WB
反应: Human, Mouse, Rat
预测: Pig, Bovine, Horse, Sheep, Rabbit, Dog, Chicken, Xenopus
蛋白号: Q96FJ2
RRID: AB_2845927

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   规格 价格 库存
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human, Mouse, Rat
克隆:
Polyclonal
特异性:
DYNLL2 Antibody detects endogenous levels of total DYNLL2.
RRID:
AB_2845927
引用格式: Affinity Biosciences Cat# DF12966, RRID:AB_2845927.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

8 kDa dynein light chain b; C87222; cytoplasmic; Dlc2; DLC8b; DNCL1B; DYL2_HUMAN; Dynein light chain 2; Dynein light chain 2, cytoplasmic; Dynein light chain LC8 type 2; Dynein light chain LC8-type 2; Dynll2; MGC17810; MGC72334;

抗原和靶标

免疫原:

A synthesized peptide derived from human DYNLL2, corresponding to a region within N-terminal amino acids.

基因/基因ID:

研究领域

· Organismal Systems > Excretory system > Vasopressin-regulated water reabsorption.

文献引用

1). Post-testicular spermatozoa of a marine teleost can conduct de novo cytoplasmic and mitochondrial translation. iScience, 2024 (PubMed: 39801836) [IF=5.8]

Application: WB    Species: fish    Sample:

Figure 7 Immunostaining and immunoblot of ribosomal and motility-related proteins in SPZED and SPZEJ (A–F) The upper panels show representative immunostaining of large ribosomal subunit protein eL31 (Rpl31, A), small ribosomal subunit protein uS5 (Rps2, B), 40S ribosomal protein S13 (Rps13, C), sperm-associated antigen 6 (Spag6, D), dynein light chain 2 (Dynll2, E) and α-tubulin (Tuba, F) in SPZED and SPZEJ. The brightfield (left) and epifluorescence (right) images with the nucleus counterstained with DAPI (blue) are shown. Scale bars, 5 μm. The lower panels depict the corresponding immunoblots (left) and quantitation normalized to prohibitin (Phb) or histone H3 (H3) (right). The data points (red dots) are presented as box and whisker plots/scatter dots with horizontal line (inside box) indicating median and outliers (n = 3–4 fish different from those employed for MS analyses). Statistical differences in protein abundance between SPZED and SPZEJ were determined by an unpaired Student’s t test (p-values indicated above each plot). Molecular mass markers (kDa) are on the left, and the corresponding MS quantification data are presented below the plots. (G and H) Representative immunostaining of small mitochondrial ribosomal subunit uS5m (mRps5, A) and large mitochondrial ribosomal subunit bL28m (mRpl28, B) in SPZED and SPZEJ. The nucleus was counterstained with 4′,6-diamidino-2-phenylindole dihydrochloride (DAPI; blue), whereas the spermatozoon mitochondrion was labeled with MitoTracker Green FM (green). Scale bars, 5 μm. To the right of each panel the corresponding immunoblots using PhB as loading control are shown. Molecular mass markers (kDa) are on the left.

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